Details for New Drug Application (NDA): 076756
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The generic ingredient in METFORMIN HYDROCHLORIDE is metformin hydrochloride. There are forty-nine drug master file entries for this compound. Eighty-two suppliers are listed for this compound. Additional details are available on the metformin hydrochloride profile page.
Summary for 076756
| Tradename: | METFORMIN HYDROCHLORIDE |
| Applicant: | Nostrum Pharms Llc |
| Ingredient: | metformin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 076756
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 076756 | ANDA | Bryant Ranch Prepack | 63629-9147 | 63629-9147-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9147-1) |
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 076756 | ANDA | Bryant Ranch Prepack | 71335-9683 | 71335-9683-1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
| Approval Date: | Jul 26, 2006 | TE: | AB1 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 750MG | ||||
| Approval Date: | Dec 12, 2011 | TE: | AB | RLD: | No | ||||
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