Details for New Drug Application (NDA): 074151
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NDA 074151 describes CIMETIDINE, which is a drug marketed by Apotex, Chartwell Molecules, Chartwell Rx, Contract Pharmacal, Cycle, Hikma, Ivax Sub Teva Pharms, L Perrigo Co, Mylan, Novitium Pharma, Perrigo, Pliva, Sandoz, Teva, Upsher Smith Labs, Watson Labs Inc, Watson Labs Teva, Cosette, Endo Operations, Hospira, Luitpold, Teva Parenteral, Ani Pharms, Chartwell Molecular, G And W Labs Inc, Pai Holdings Pharm, Pharm Assoc, and Pharmobedient Cnsltg, and is included in forty-nine NDAs. It is available from sixteen suppliers. Additional details are available on the CIMETIDINE profile page.
The generic ingredient in CIMETIDINE is cimetidine hydrochloride. There are twenty-five drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the cimetidine hydrochloride profile page.
The generic ingredient in CIMETIDINE is cimetidine hydrochloride. There are twenty-five drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the cimetidine hydrochloride profile page.
Summary for 074151
| Tradename: | CIMETIDINE |
| Applicant: | Teva |
| Ingredient: | cimetidine |
| Patents: | 0 |
Pharmacology for NDA: 074151
| Mechanism of Action | Histamine H2 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 074151
Suppliers and Packaging for NDA: 074151
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CIMETIDINE | cimetidine | TABLET;ORAL | 074151 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-8192 | 0093-8192-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-8192-01) |
| CIMETIDINE | cimetidine | TABLET;ORAL | 074151 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-8192 | 0093-8192-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-8192-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
| Approval Date: | May 17, 1994 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 300MG | ||||
| Approval Date: | May 17, 1994 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 400MG | ||||
| Approval Date: | May 17, 1994 | TE: | AB | RLD: | No | ||||
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