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METFORMIN HYDROCHLORIDE
METFORMIN HYDROCHLORIDE - 62584-332-01 - (METFORMIN HYDROCHLORIDE)
Drug Information of METFORMIN HYDROCHLORIDE
| Product NDC: | 62584-332 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METFORMIN HYDROCHLORIDE
| Product NDC: | 62584-332 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077064 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091118 |
Package Information of METFORMIN HYDROCHLORIDE
| Package NDC: | 62584-332-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (62584-332-01) > 10 TABLET in 1 BLISTER PACK (62584-332-11) |
NDC Information of METFORMIN HYDROCHLORIDE
| NDC Code | 62584-332-01 |
| Proprietary Name | METFORMIN HYDROCHLORIDE |
| Package Description | 10 BLISTER PACK in 1 CARTON (62584-332-01) > 10 TABLET in 1 BLISTER PACK (62584-332-11) |
| Product NDC | 62584-332 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METFORMIN HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091118 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 850 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
