Details for New Drug Application (NDA): 203769
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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-six suppliers are listed for this compound. Additional details are available on the metformin hydrochloride profile page.
Summary for 203769
| Tradename: | METFORMIN HYDROCHLORIDE |
| Applicant: | Sciegen Pharms Inc |
| Ingredient: | metformin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 203769
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET;ORAL | 203769 | ANDA | Aphena Pharma Solutions - Tennessee, LLC | 43353-082 | 43353-082-30 | 30 TABLET in 1 BOTTLE (43353-082-30) |
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET;ORAL | 203769 | ANDA | Aphena Pharma Solutions - Tennessee, LLC | 43353-082 | 43353-082-53 | 60 TABLET in 1 BOTTLE (43353-082-53) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
| Approval Date: | Sep 11, 2013 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 850MG | ||||
| Approval Date: | Sep 11, 2013 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 1GM | ||||
| Approval Date: | Sep 11, 2013 | TE: | AB | RLD: | No | ||||
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