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Metformin Hydrochloride
Metformin Hydrochloride - 0591-2720-60 - (Metformin Hydrochloride)
Drug Information of Metformin Hydrochloride
| Product NDC: | 0591-2720 |
| Proprietary Name: | Metformin Hydrochloride |
| Non Proprietary Name: | Metformin Hydrochloride |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Metformin Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metformin Hydrochloride
| Product NDC: | 0591-2720 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021574 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120418 |
Package Information of Metformin Hydrochloride
| Package NDC: | 0591-2720-60 |
| Package Description: | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-2720-60) |
NDC Information of Metformin Hydrochloride
| NDC Code | 0591-2720-60 |
| Proprietary Name | Metformin Hydrochloride |
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-2720-60) |
| Product NDC | 0591-2720 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metformin Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120418 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
