Details for New Drug Application (NDA): 091664
The generic ingredient in METFORMIN HYDROCHLORIDE is metformin hydrochloride. There is one drug master file entry for this compound. Eighty-two suppliers are listed for this compound. Additional details are available on the metformin hydrochloride profile page.
Summary for 091664
| Tradename: | METFORMIN HYDROCHLORIDE |
| Applicant: | Lupin |
| Ingredient: | metformin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 091664
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 091664 | ANDA | Lupin Pharmaceuticals, Inc. | 68180-338 | 68180-338-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-338-01) |
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 091664 | ANDA | Lupin Pharmaceuticals, Inc. | 68180-339 | 68180-339-09 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-339-09) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
| Approval Date: | Jul 19, 2013 | TE: | AB3 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 1GM | ||||
| Approval Date: | Jul 19, 2013 | TE: | AB3 | RLD: | No | ||||
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