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FAMOTIDINE IV INJECTION 10 MG — DIN 02247800

FAMOTIDINE : 10 MG · TEVA CANADA LIMITED · SOLUTION · wholesale supply in Canada

Health Canada status: CANCELLED PRE MARKET

What is FAMOTIDINE IV INJECTION?

FAMOTIDINE IV INJECTION 10 MG contains FAMOTIDINE : 10 MG. It is listed in the Health Canada Drug Product Database under DIN 02247800, held by TEVA CANADA LIMITED, supplied as SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as cancelled pre market, status dated 16-Oct-2015. This Drug Identification Number is no longer authorized for sale in Canada, so Nexara does not supply it. The record is kept here because buyers still meet the number on old formularies, purchase orders and tender documents; Nexara can help identify an authorized alternative.

What is FAMOTIDINE IV INJECTION used for?

Acute duodenal/benign gastric ulcer; prophylaxis of duodenal ulcer; pathological hypersecretory conditions (e.g. Zollinger-Ellison); GERD; maintenance of remission of GERD.

Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.

How much does Famotidine cost around the world?

Famotidine is listed on 11 of the national price registers Nexara ingests. Each country publishes on a different basis, so figures are not comparable with one another — or with a Canadian wholesale price.

What a market publishes matters more than the number it publishes. Australia publishes a ex-manufacturer; Austria publishes a KVP (Kassenverkaufspreis); Bahrain publishes a retail (max). Comparing an ex-factory ceiling against a pharmacy public price tells you nothing about either, and comparing either against a Canadian landed cost tells you less.

MarketPrice basis published thereBrandsPacks listed
United Statesacquisition5112
Saudi Arabiapublic1121
AustriaKVP (Kassenverkaufspreis)918
Czechiamax producer price (ex-factory)27
Bahrainretail (max)36
Greeceproducer price (ex-factory)66
Australiaex-manufacturer24
MoroccoPPV (public price)34
United Arab Emiratespublic22
United Kingdomhospital22
Icelandmax wholesale22

184 pack listings across 47 brand entries and 10 price bases, refreshed 10 Sep 2026. Ranges span every Famotidine pack in that market, so a high figure is usually a larger pack rather than the same product.

This table is a regulatory record of where the molecule is listed. The DIN on this page is no longer authorized for sale in Canada, so Nexara does not quote it — see the alternatives above.

Is there a generic Famotidine in Canada, and who makes it?

Every market authorization holder with a Canadian DIN for this molecule, and how many of their listings Health Canada currently shows as marketed.

27 holders have a Canadian DIN containing Famotidine, across 68 DINs, of which 17 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.

Market authorization holderDINsMarketedBrand namesPosition
ANGITA PHARMA INC.33ACID CONTROLLER MAXIMUM STRENGTH, AG-FAMOTIDINESourceable in Canada
TEVA CANADA LIMITED82ACID CONTROL, FAMOTIDINE (ACID CONTROLLER) TABLETS, FAMOTIDINE IV INJECTION, NTP-FAMOTIDINE, TEVA-FAMOTIDINESourceable in Canada
MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC32MAXIMUM STRENGTH PEPCID AC, PEPCID ACSourceable in Canada
JAMP PHARMA CORPORATION22JAMP FAMOTIDINESourceable in Canada
MINT PHARMACEUTICALS INC22MINT-FAMOTIDINESourceable in Canada
OMEGA LABORATORIES LIMITED22FAMOTIDINE OMEGA -(WITH PRESERVATIVE,BENZYL ALCOHOL), FAMOTIDINE OMEGA -(WITHOUT PRESERVATIVE)Sourceable in Canada
SANIS HEALTH INC22FAMOTIDINESourceable in Canada
SIVEM PHARMACEUTICALS ULC22FAMOTIDINESourceable in Canada
APOTEX INC80ACID CONTROL, APO-FAMOTIDINE, APO-FAMOTIDINE INJECTABLE, APO-FAMOTIDINE TAB 20MG USP, APO-FAMOTIDINE TAB 40MG USP, +1 moreNo marketed DIN
MYLAN PHARMACEUTICALS ULC50FAMOTIDINE INJECTION, MYLAN-FAMOTIDINE, PEPTIC GUARDNo marketed DIN
MERCK CANADA INC40PEPCID AC (CHEWABLE TAB) - 10MG, PEPCID I.V. 10MG/ML, PEPCID TAB 20MG, PEPCID TAB 40MGNo marketed DIN
AURO PHARMA INC30AURO-FAMOTIDINE 10 MG, AURO-FAMOTIDINE 20 MG, AURO-FAMOTIDINE MINT 20 MGNo marketed DIN

Health Canada’s Drug Product Database does not flag which listing is the originator and which are subsequent-entry products, so Nexara does not label them here. Interchangeability is determined provincially, not federally — confirm for your province before a formulary switch. Nexara can confirm which of these is actually obtainable, and on what lead time, per order.

How is it supplied and stored?

Pack configuration, storage class and the handling constraints that drive cold-chain planning. One DIN can cover more than one pack size, and the pack — not the DIN — is what gets priced, shipped and invoiced.

Strength on the label10 MG
Dosage formSOLUTION
RouteINTRAVENOUS
Pack configuration (monograph)Tablets: Bottles of 100, 500; unit dose 30, 100. Injection: 2 mL single-use vials; 4 mL, 20 mL multidose vials; 50 mL Pharmacy Bulk vials.
StorageTablets: 15-30°C, light-resistant. Injection: 2°C to 8°C, protect from light, do not freeze. Diluted IV solution: use within 24 hours.

Pack detail is kept as a regulatory record. This DIN is no longer authorized for sale in Canada, so Nexara does not quote this pack.

Substance and classification

Active substanceFamotidine
ATC codeA02BA03
AHFS class56:28.12
Biosimilar biologicNo

Health Canada record and identifiers

The regulatory facts straight from the Drug Product Database, plus every identifier form Nexara accepts on a purchase order. A DIN written without its leading zeros is the commonest reason an order line fails to match.

DIN (8-digit, as used in ordering)02247800
DIN (unpadded, as printed on some documents)2247800
Brand nameFAMOTIDINE IV INJECTION
Generic / active ingredientFAMOTIDINE : 10 MG
Market authorization holderTEVA CANADA LIMITED
Health Canada schedulePrescription
ATC codeA02BA03
ATC anatomical main groupA — Alimentary tract and metabolism
ATC therapeutic subgroupA02BA
Current statusCANCELLED PRE MARKET
Status date16-Oct-2015
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

How is it administered?

Duodenal/Gastric Ulcer: 40 mg at bedtime. GERD: 20-40 mg twice daily. IV: 20 mg every 12 hours. Adjust dose in moderate/severe renal insufficiency (reduce dose by half or extend interval to 36-48h).

Included because it drives pack selection and wastage. Consult the monograph.

Contraindications

Hypersensitivity to famotidine or any component of the medication. Cross-sensitivity with other H2-receptor antagonists has been observed.

Warnings and precautions

Exclude gastric malignancy before treating gastric ulcers. CNS adverse effects reported in patients with moderate to severe renal insufficiency. Contains benzyl alcohol (multidose vials).

Is Famotidine in shortage in Canada?

A Canadian shortage report is on file for a product containing this molecule: Active — reported by OMEGA LABORATORIES LIMITED (Tier 3 shortage FAMOTIDINE OMEGA -(WITHOUT PRESERVATIVE)" aria-label="Actual Tier 3 shortage FAMOTIDINE OMEGA -(WITHOUT), last seen 09 Sep 2026. A shortage on one presentation does not always affect every DIN of the molecule — the alternatives below list what else is marketed in Canada. Nexara can confirm current availability and identify substitutions or import options where permitted.

Check availability for FAMOTIDINE IV INJECTION

What can be used instead?

Alternatives on every axis a buyer actually considers — the same molecule in another presentation, the same class, an adjacent class, or a fixed-dose combination. Every row is led by the marketed DIN count, because that is what can be bought this week.

1 · Same molecule, other Canadian presentations

17 of 68 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
ACID CONTROLLER MAXIMUM STRENGTH20 MGTABLETANGITA PHARMA INC.MARKETED02538350
AG-FAMOTIDINE20 MGTABLETANGITA PHARMA INC.MARKETED02509970
AG-FAMOTIDINE40 MGTABLETANGITA PHARMA INC.MARKETED02509989
FAMOTIDINE40 MGTABLETSIVEM PHARMACEUTICALS ULCMARKETED02549115
FAMOTIDINE40 MGTABLETSANIS HEALTH INCMARKETED02351110
FAMOTIDINE20 MGTABLETSANIS HEALTH INCMARKETED02351102
FAMOTIDINE20 MGTABLETSIVEM PHARMACEUTICALS ULCMARKETED02549107
FAMOTIDINE OMEGA -(WITH PRESERVATIVE,BENZYL ALCOHOL)10 MGSOLUTIONOMEGA LABORATORIES LIMITEDMARKETED02247745
FAMOTIDINE OMEGA -(WITHOUT PRESERVATIVE)10 MGSOLUTIONOMEGA LABORATORIES LIMITEDMARKETED02247735
JAMP FAMOTIDINE40 MGTABLETJAMP PHARMA CORPORATIONMARKETED02507757

2 · Same class — other molecules in ATC A02BA

MoleculeCanadian brandsDINsMarketedSourceable
FamotidineACID CONTROL · ACID CONTROLLER MAXIMUM STRENGTH · ACT · AG-FAMOTIDINE · +39 more6817Yes
RanitidineACID REDUCER · ACID REDUCER MAXIMUM STRENGTH NON-PRESCRIPTION · ACT RANITIDINE · AG-RANITIDINE · +46 more965Yes
CimetidineAPO-CIMETIDINE ORAL SOLUTION · CIMETIDINE · CIMETIDINE 200 TAB 200MG · CIMETIDINE TAB 300MG · +27 more502Yes
NizatidineAPO-NIZATIDINE · AXID · DOM-NIZATIDINE 150MG CAPSULES · GEN-NIZATIDINE · +7 more191Yes
Famotidine, CombinationsPEPCID COMPLETE11Yes
Ranitidine Bismuth CitratePYLORID10Not in Canada

A molecule with zero marketed DINs cannot be sourced domestically, however many approvals it holds — if one of these sits on a formulary or in an older protocol, that is the line to check.

3 · Adjacent classes in ATC A02B

ATC subgroupMoleculesDINsMarketed
A02BCDexlansoprazole · Esomeprazole · Lansoprazole · Omeprazole · Pantoprazole · +1 more288108
A02BXAlginic Acid · Pirenzepine · Sucralfate324
A02BBMisoprostol102
A02BDBismuth Subcitrate,Tetracycline And Metronidazole · Lansoprazole, Amoxicillin And Clarithromycin32

Not clinical advice. These tables describe what can be supplied in Canada, not what should be prescribed. Substitution within or across classes is a prescriber and pharmacist decision, and interchangeability is determined provincially.

What else is FAMOTIDINE IV INJECTION called?

The same molecule, Famotidine, is registered under other names elsewhere. Buyers and prescribers searching from outside Canada — or working from a foreign prescription or tender document — often know it by one of these:

NameScriptRegistered in
FAMOSANLatinCzechia
famodarLatinBahrain, Saudi Arabia
Famotidine AmaroxLatinSaudi Arabia
FAMOGENLatinSaudi Arabia
FAMOPSINLatinBahrain
ULCERANLatinBahrain
FamodineLatinSaudi Arabia
Famotidin GenericonLatinIceland
Famotidin STADALatinIceland
Famotidine for oral suspensionLatinSaudi Arabia
QUAMATELLatinCzechia
ULCIDINELatinMorocco

Names are taken from national medicine registers and published price lists. A product registered abroad is not authorized for sale in Canada unless it holds its own DIN; import is possible only through the routes Health Canada permits.

What is Famotidine called in other languages?

Buyers, prescribers and procurement teams outside Canada often search for the ingredient in their own script. These are phonetic renderings of the ingredient name Famotidine, published to help those searches reach this page.

LanguageFamotidine
Arabic العربيةفاموتيدين
Chinese (Simplified) 简体中文法莫替丁
Russian Русскийфамотидин
Spanish Españolfamotidina
French Françaisfamotidine
Portuguese Portuguêsfamotidina
German DeutschFamotidin
Persian فارسیفاموتیدین
Turkish Türkçefamotidin
Japanese 日本語ファモチジン
Thai ไทยฟาโมทิดีน
Indonesian Bahasa Indonesiafamotidin
Hebrew עבריתפמוטידין
Italian Italianofamotidina

These are transliterations of the ingredient name, generated automatically and published only where two independent checks agreed. They are not registered local trade names and carry no marketing authorisation in any market. Always confirm a product against its local registration before ordering.

Can this still be bought in Canada?

No. This Drug Identification Number is cancelled pre market in Health Canada's Drug Product Database, so the product is no longer authorized for sale in Canada and Nexara does not supply it. This page is kept as a regulatory record.

If you are looking for a current equivalent, the alternatives above list every product sharing this therapeutic class, with the marketed ones first. Ask us to source an alternative

Ordering questions

Who can buy this from Nexara?

Licensed entities only. Nexara holds Health Canada establishment licence DEL 3-002896-A and ships only to a licensed address. Patients and unlicensed buyers are routed to a partner pharmacy.

Is there a minimum order?

Yes, set per product line and per pack multiple rather than on the order total, so you are never asked to buy a part-pack. The minimum for this line is confirmed with your quote.

What is the lead time?

Confirmed per order at quotation, and it depends on current stock position and whether the product is in shortage.

Why is there no price on this page?

Nexara quotes a delivered Canadian price per order, against a verified licence. Foreign list prices are published on incompatible bases and are not a guide to what any buyer can obtain here, so this page shows which markets list the molecule and on what basis, and nothing more.

Can Nexara supply this for a clinical trial?

Yes — comparator and background-therapy supply, including sourcing from other markets where a Canadian pack will not satisfy the protocol. Clinical trial supply.

Sources and disclaimer

Product data sourced from the Health Canada Drug Product Database and the approved product monograph (PDF). Health Canada status reconciled against the live DPD sync. Last reviewed 11 Sep 2026.

Nothing on this page is medical advice. Nexara Health is a licensed wholesale distributor and supplies licensed entities only; consumer orders are routed to a partner pharmacy. Alternatives tables describe supply, not clinical equivalence.

Health Canada Drug Product Database (DPD), DIN 02247800. Last reviewed 2026-09-11. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.