Product NDC: | 54868-4564 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-4564 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075967 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020130 |
Package NDC: | 54868-4564-6 |
Package Description: | 120 TABLET in 1 BOTTLE (54868-4564-6) |
NDC Code | 54868-4564-6 |
Proprietary Name | Metformin Hydrochloride |
Package Description | 120 TABLET in 1 BOTTLE (54868-4564-6) |
Product NDC | 54868-4564 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metformin hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20020130 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | METFORMIN HYDROCHLORIDE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |