Details for New Drug Application (NDA): 077880
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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 077880
| Tradename: | METFORMIN HYDROCHLORIDE |
| Applicant: | Amneal Pharms Ny |
| Ingredient: | metformin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 077880
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET;ORAL | 077880 | ANDA | PD-Rx Pharmaceuticals, Inc. | 43063-527 | 43063-527-14 | 14 TABLET in 1 BOTTLE, PLASTIC (43063-527-14) |
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET;ORAL | 077880 | ANDA | PD-Rx Pharmaceuticals, Inc. | 43063-527 | 43063-527-20 | 20 TABLET in 1 BOTTLE, PLASTIC (43063-527-20) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
| Approval Date: | Jun 5, 2006 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 850MG | ||||
| Approval Date: | Jun 5, 2006 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 1GM | ||||
| Approval Date: | Jun 5, 2006 | TE: | RLD: | No | |||||
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