Product NDC: | 0904-5849 |
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: | 0904-5849 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075985 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020125 |
Package NDC: | 0904-5849-54 |
Package Description: | 450 TABLET, FILM COATED in 1 BOTTLE (0904-5849-54) |
NDC Code | 0904-5849-54 |
Proprietary Name | Metformin Hydrochloride |
Package Description | 450 TABLET, FILM COATED in 1 BOTTLE (0904-5849-54) |
Product NDC | 0904-5849 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metformin Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20020125 |
Marketing Category Name | ANDA |
Labeler Name | Major Pharmaceuticals |
Substance Name | METFORMIN HYDROCHLORIDE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |