Details for New Drug Application (NDA): 203832
✉ Email this page to a colleague
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 203832
| Tradename: | METFORMIN HYDROCHLORIDE |
| Applicant: | Mpp Pharma |
| Ingredient: | metformin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 203832
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 203832 | ANDA | Golden State Medical Supply, Inc. | 51407-059 | 51407-059-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-059-60) |
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 203832 | ANDA | Westminster Pharmaceuticals, LLC | 69367-412 | 69367-412-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69367-412-60) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
| Approval Date: | Dec 26, 2017 | TE: | AB2 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 1GM | ||||
| Approval Date: | Dec 26, 2017 | TE: | AB2 | RLD: | No | ||||
Complete Access Available with Subscription
