Product NDC: | 60429-280 |
Proprietary Name: | Metformin Hydrochloride |
Non Proprietary Name: | Metformin Hydrochloride ER |
Active Ingredient(s): | 750 mg/1 & nbsp; Metformin Hydrochloride ER |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60429-280 |
Labeler Name: | Golden State Medical Supply, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076869 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060412 |
Package NDC: | 60429-280-10 |
Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (60429-280-10) |
NDC Code | 60429-280-10 |
Proprietary Name | Metformin Hydrochloride |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (60429-280-10) |
Product NDC | 60429-280 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metformin Hydrochloride ER |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20060412 |
Marketing Category Name | ANDA |
Labeler Name | Golden State Medical Supply, Inc. |
Substance Name | METFORMIN HYDROCHLORIDE |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |