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METFORMIN HYDROCHLORIDE
METFORMIN HYDROCHLORIDE - 68382-029-30 - (METFORMIN HYDROCHLORIDE)
Drug Information of METFORMIN HYDROCHLORIDE
| Product NDC: | 68382-029 |
| Proprietary Name: | METFORMIN HYDROCHLORIDE |
| Non Proprietary Name: | METFORMIN HYDROCHLORIDE |
| Active Ingredient(s): | 850 mg/1 & nbsp; METFORMIN HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METFORMIN HYDROCHLORIDE
| Product NDC: | 68382-029 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077064 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050928 |
Package Information of METFORMIN HYDROCHLORIDE
| Package NDC: | 68382-029-30 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68382-029-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of METFORMIN HYDROCHLORIDE
| NDC Code | 68382-029-30 |
| Proprietary Name | METFORMIN HYDROCHLORIDE |
| Package Description | 10 BLISTER PACK in 1 CARTON (68382-029-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 68382-029 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METFORMIN HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050928 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 850 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
