Product NDC: | 67046-460 |
Proprietary Name: | METFORMIN HYDROCHLORIDE |
Non Proprietary Name: | METFORMIN HYDROCHLORIDE |
Active Ingredient(s): | 500 mg/1 & nbsp; METFORMIN HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67046-460 |
Labeler Name: | Contract Pharmacy Services-PA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077064 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100409 |
Package NDC: | 67046-460-30 |
Package Description: | 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-460-30) |
NDC Code | 67046-460-30 |
Proprietary Name | METFORMIN HYDROCHLORIDE |
Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-460-30) |
Product NDC | 67046-460 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METFORMIN HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100409 |
Marketing Category Name | ANDA |
Labeler Name | Contract Pharmacy Services-PA |
Substance Name | METFORMIN HYDROCHLORIDE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |