Details for New Drug Application (NDA): 206955
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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 206955
| Tradename: | METFORMIN HYDROCHLORIDE |
| Applicant: | Macleods Pharms Ltd |
| Ingredient: | metformin hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 206955
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 206955 | ANDA | Macleods Pharmaceuticals Limited | 33342-239 | 33342-239-11 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-239-11) |
| METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 206955 | ANDA | Macleods Pharmaceuticals Limited | 33342-240 | 33342-240-11 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-240-11) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
| Approval Date: | Dec 7, 2016 | TE: | AB1 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 750MG | ||||
| Approval Date: | Dec 7, 2016 | TE: | AB | RLD: | No | ||||
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