Details for New Drug Application (NDA): 212681
✉ Email this page to a colleague
The generic ingredient in METFORMIN HYDROCHLORIDE is metformin hydrochloride; saxagliptin hydrochloride. There are forty-nine drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the metformin hydrochloride; saxagliptin hydrochloride profile page.
Summary for 212681
Tradename: | METFORMIN HYDROCHLORIDE |
Applicant: | Prinston Inc |
Ingredient: | metformin hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 212681
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 212681 | ANDA | Solco Healthcare US, LLC. | 43547-503 | 43547-503-10 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-503-10) |
METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 212681 | ANDA | Solco Healthcare US, LLC. | 43547-503 | 43547-503-50 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-503-50) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
Approval Date: | Jun 9, 2022 | TE: | AB3 | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 1GM | ||||
Approval Date: | Jun 9, 2022 | TE: | AB3 | RLD: | No |
Complete Access Available with Subscription