Home
>
National Drug Code (NDC)
>
Metformin Hydrochloride
Metformin Hydrochloride - 50268-531-15 - (Metformin Hydrochloride)
Drug Information of Metformin Hydrochloride
| Product NDC: | 50268-531 |
| 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, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metformin Hydrochloride
| Product NDC: | 50268-531 |
| Labeler Name: | AvPAK |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078596 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091202 |
Package Information of Metformin Hydrochloride
| Package NDC: | 50268-531-15 |
| Package Description: | 50 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (50268-531-15) |
NDC Information of Metformin Hydrochloride
| NDC Code | 50268-531-15 |
| Proprietary Name | Metformin Hydrochloride |
| Package Description | 50 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (50268-531-15) |
| Product NDC | 50268-531 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metformin Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091202 |
| Marketing Category Name | ANDA |
| Labeler Name | AvPAK |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
