PHL-RANITIDINE 300 MG
RANITIDINE (RANITIDINE HYDROCHLORIDE) : 300 MG · DIN 02245783 · PHARMEL INC
Health Canada status: CANCELLED POST MARKET
What is PHL-RANITIDINE?
PHL-RANITIDINE 300 MG contains RANITIDINE (RANITIDINE HYDROCHLORIDE) : 300 MG. It is listed in the Health Canada Drug Product Database under DIN 02245783, held by PHARMEL INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 01-Sep-2009. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A) and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.
What is PHL-RANITIDINE used for?
Treatment of duodenal ulcer, benign gastric ulcer, reflux esophagitis, post-operative peptic ulcer, Zollinger-Ellison Syndrome, NSAID-induced lesions, and prophylaxis of GI haemorrhage.
Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.
Product details and regulatory record
| DIN | 02245783 |
|---|---|
| Brand name | PHL-RANITIDINE |
| Generic / active ingredient | RANITIDINE (RANITIDINE HYDROCHLORIDE) : 300 MG |
| Manufacturer | PHARMEL INC |
| Strength | 300 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | A02BA02 RANITIDINE |
| AHFS class | 56:28.12 |
| Biosimilar | No |
| Health Canada status | CANCELLED POST MARKET |
| Status date | 01-Sep-2009 |
| Original market date | 2002-08-27 00:00:00 |
How is it administered?
Duodenal/gastric ulcer: 300 mg at bedtime or 150 mg BID. Reflux esophagitis: 150 mg BID or 300 mg at bedtime. Maintenance: 150 mg at bedtime. Adjust dose in severe renal impairment.
Included because it drives pack selection and wastage. Consult the monograph.
How is it stored and handled?
Store at controlled room temperature 15 - 30°C. Protect from light and moisture.
How is it supplied?
150 mg: Bottles of 60, 100, 500, 1000; blisters of 10, 30. 300 mg: Bottles of 30, 100, 500; blisters of 10, 30.
Contraindications
Known hypersensitivity to ranitidine. Avoid in patients with a history of acute porphyria.
Warnings and precautions
Exclude gastric malignancy before therapy. Supervision recommended with concomitant NSAID use. May precipitate acute porphyric attacks. Elderly at risk for confusion.
What can be used instead?
Other Canadian products sharing ATC code A02BA02 RANITIDINE. 5 of 96 DINs in this group are currently marketed — marketed products are listed first, because that is what can actually be bought. These tables describe supply, not clinical equivalence: substitution rests with the prescriber or pharmacist, and interchangeability is determined provincially.
| Product | Strength | Form | Manufacturer | Health Canada status | DIN |
|---|---|---|---|---|---|
| MAR-RANITIDINE | 150 MG | TABLET | MARCAN PHARMACEUTICALS INC | MARKETED | DIN 02443708 |
| MAR-RANITIDINE | 300 MG | TABLET | MARCAN PHARMACEUTICALS INC | MARKETED | DIN 02443716 |
| MAXIMUM STRENGTH ACID REDUCER WITHOUT PRESCRIPTION | 150 MG | TABLET | PHARMASCIENCE INC | MARKETED | DIN 02293471 |
| MINT-RANITIDINE | 150 MG | TABLET | MINT PHARMACEUTICALS INC | MARKETED | DIN 02526379 |
| MINT-RANITIDINE | 300 MG | TABLET | MINT PHARMACEUTICALS INC | MARKETED | DIN 02526387 |
| ACID REDUCER | 150 MG | TABLET | APOTEX INC | DORMANT | DIN 02296160 |
| ACID REDUCER | 150 MG | TABLET | PENDOPHARM DIVISION OF PHARMASCIENCE INC | APPROVED | DIN 02291282 |
| ACID REDUCER | 150 MG | TABLET | PHARMASCIENCE INC | CANCELLED POST MARKET | DIN 02400103 |
| ACID REDUCER | 75 MG | TABLET | MYLAN PHARMACEUTICALS ULC | CANCELLED POST MARKET | DIN 02237829 |
| ACID REDUCER | 75 MG | TABLET | APOTEX INC | DORMANT | DIN 02230507 |
Who else supplies RANITIDINE worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. RANITIDINE appears in 4061 registered pack listings across 3 markets, published on 3 different national price bases. Where a Canadian route is closed, that is where an alternative route of supply starts — subject to the import rules in both countries.
Registered listings are not stock. Ask us to confirm what can actually be sourced for your order.
How can I get it?
Nexara Health supplies this product to licensed Canadian buyers — pharmacies, hospitals, clinics, licensed distributors, and clinical trial sponsors or their CROs. We confirm stock, pack size, expiry and pricing at the time of quotation. If the product is on backorder or in shortage, we identify equivalent alternatives and import options where permitted.
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.
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.
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.