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SANDOZ AMPHETAMINE XR 30 MG — DIN 02457342

MIXED SALTS AMPHETAMINE : 30 MG · SANDOZ CANADA INCORPORATED · CAPSULE (EXTENDED RELEASE) · wholesale supply in Canada

Health Canada status: CANCELLED POST MARKET

What is SANDOZ AMPHETAMINE XR?

SANDOZ AMPHETAMINE XR 30 MG contains MIXED SALTS AMPHETAMINE : 30 MG. It is listed in the Health Canada Drug Product Database under DIN 02457342, held by SANDOZ CANADA INCORPORATED, supplied as CAPSULE (EXTENDED RELEASE) for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 31-Jul-2026. 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 SANDOZ AMPHETAMINE XR used for?

SANDOZ AMPHETAMINE XR (mixed salts amphetamine extended-release capsules) is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in: Children (6 – 12 years of age), Adolescents (13 – 17 years of age), Adults (18 years of age or older). SANDOZ AMPHETAMINE XR is indicated as an integral part of a total treatment program for ADHD that may include other measures (psychological, educational, social) for patients with this syndrome.

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

Is there a generic Amfetamine 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.

7 holders have a Canadian DIN containing Amfetamine, across 41 DINs, of which 22 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.

Market authorization holderDINsMarketedBrand namesPosition
APOTEX INC66APO-AMPHETAMINE XRSourceable in Canada
TAKEDA CANADA INC66ADDERALL XRSourceable in Canada
TEVA CANADA LIMITED66TEVA-AMPHETAMINE XRSourceable in Canada
KYE PHARMACEUTICALS INC.54DYANAVEL XRSourceable in Canada
PHARMASCIENCE INC60PMS-AMPHETAMINES XRNo marketed DIN
SANDOZ CANADA INCORPORATED60SANDOZ AMPHETAMINE XRNo marketed DIN
SUN PHARMA CANADA INC60TARO-AMPHETAMINE XRNo 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 label30 MG
Dosage formCAPSULE (EXTENDED RELEASE)
RouteORAL
Pack configuration (monograph)SANDOZ AMPHETAMINE XR 5 mg Capsules: Bottles of 100. SANDOZ AMPHETAMINE XR 10 mg Capsules: Bottles of 100. SANDOZ AMPHETAMINE XR 15 mg Capsules: Bottles of 100. SANDOZ AMPHETAMINE XR 20 mg Capsules: Bottles of 100. SANDOZ AMPHETAMINE XR 25 mg Capsules: Bottles of 100. SANDOZ AMPHETAMINE XR 30 mg Capsules: Bottles of 100.

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 substanceAmfetamine
ATC codeN06BA01
AHFS class84:92.00 ; 84:06.00
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)02457342
DIN (unpadded, as printed on some documents)2457342
Brand nameSANDOZ AMPHETAMINE XR
Generic / active ingredientMIXED SALTS AMPHETAMINE : 30 MG
Market authorization holderSANDOZ CANADA INCORPORATED
Health Canada scheduleCONTROLLED DRUGS (CDSA I)
ATC codeN06BA01
ATC anatomical main groupN — Nervous system
ATC therapeutic subgroupN06BA
Current statusCANCELLED POST MARKET
Status date31-Jul-2026
Original market date2016-11-11 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

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

22 of 41 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
ADDERALL XR20 MGCAPSULE (EXTENDED RELEASE)TAKEDA CANADA INCMARKETED02248811
ADDERALL XR5 MGCAPSULE (EXTENDED RELEASE)TAKEDA CANADA INCMARKETED02248808
ADDERALL XR25 MGCAPSULE (EXTENDED RELEASE)TAKEDA CANADA INCMARKETED02248812
ADDERALL XR10 MGCAPSULE (EXTENDED RELEASE)TAKEDA CANADA INCMARKETED02248809
ADDERALL XR30 MGCAPSULE (EXTENDED RELEASE)TAKEDA CANADA INCMARKETED02248813
ADDERALL XR15 MGCAPSULE (EXTENDED RELEASE)TAKEDA CANADA INCMARKETED02248810
APO-AMPHETAMINE XR10 MGCAPSULE (EXTENDED RELEASE)APOTEX INCMARKETED02445506
APO-AMPHETAMINE XR5 MGCAPSULE (EXTENDED RELEASE)APOTEX INCMARKETED02445492
APO-AMPHETAMINE XR15 MGCAPSULE (EXTENDED RELEASE)APOTEX INCMARKETED02445514
APO-AMPHETAMINE XR20 MGCAPSULE (EXTENDED RELEASE)APOTEX INCMARKETED02445522

2 · Same class — other molecules in ATC N06BA

MoleculeCanadian brandsDINsMarketedSourceable
LisdexamfetamineAG-LISDEXAMFETAMINE · APO-LISDEXAMFETAMINE · APO-LISDEXAMFETAMINE CAPSULES · APO-LISDEXAMFETAMINE CHEWABLE TABLETS · +7 more8766Yes
AtomoxetineAG-ATOMOXETINE · APO-ATOMOXETINE · ATOMOXETINE · AURO-ATOMOXETINE · +9 more9657Yes
MethylphenidateACT METHYLPHENIDATE ER · APO-METHYLPHENIDATE · APO-METHYLPHENIDATE CR · APO-METHYLPHENIDATE ER · +25 more10355Yes
AmfetamineADDERALL XR · APO-AMPHETAMINE XR · DYANAVEL XR · PMS-AMPHETAMINES XR · +3 more4122Yes
ModafinilALERTEC · APO-MODAFINIL · AURO-MODAFINIL · BIO-MODAFINIL · +6 more107Yes
DexamfetamineAPO-DEXTROAMPHETAMINE SR · DEXEDRINE · DEXEDRINE SPANSULE · DEXTROAMPHETAMINE · +2 more96Yes
SolriamfetolSUNOSI22Yes
DexmethylphenidateATTENADE30Not 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 N06B

ATC subgroupMoleculesDINsMarketed
N06BCCaffeine113
N06BXIdebenone · Other Psychostimulants30

4 · Fixed-dose combinations with Canadian supply

ProductActive ingredientsHolderStatusDIN
DYANAVEL XRAMPHETAMINE (AMPHETAMINE (COMPLEXED WITH SODIUM POLYSTYRENE SULFONATE), AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE) : 5 MGKYE PHARMACEUTICALS INC.MARKETED02559803

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 SANDOZ AMPHETAMINE XR called?

The same molecule, Amfetamine, 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
Amfetamin GlostrupLatinIceland

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 Amfetamine 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 Amfetamine, published to help those searches reach this page.

LanguageAmfetamine
Arabic العربيةأمفيتامين
Russian Русскийамфетамин
Spanish Españolanfetamina
French Françaisamphétamine
Portuguese Portuguêsanfetamina
German DeutschAmphetamin
Japanese 日本語アンフェタミン

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 post 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 12 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 02457342. Last reviewed 2026-09-12. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.