Details for New Drug Application (NDA): 205330
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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 205330
| Tradename: | METFORMIN HYDROCHLORIDE |
| Applicant: | Aarxion Anda Hlding |
| Ingredient: | metformin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 205330
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET;ORAL | 205330 | ANDA | Macleods Pharmaceuticals Limited | 33342-141 | 33342-141-10 | 90 TABLET, FILM COATED in 1 BOTTLE (33342-141-10) |
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET;ORAL | 205330 | ANDA | Macleods Pharmaceuticals Limited | 33342-141 | 33342-141-11 | 100 TABLET, FILM COATED in 1 BOTTLE (33342-141-11) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
| Approval Date: | Oct 31, 2017 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 850MG | ||||
| Approval Date: | Oct 31, 2017 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 1GM | ||||
| Approval Date: | Oct 31, 2017 | TE: | RLD: | No | |||||
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