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Metformin Hydrochloride Extended Release
Metformin Hydrochloride Extended Release - 49349-201-02 - (Metformin Hydrochloride Extended Release)
Drug Information of Metformin Hydrochloride Extended Release
| Product NDC: | 49349-201 |
| Proprietary Name: | Metformin Hydrochloride Extended Release |
| Non Proprietary Name: | Metformin Hydrochloride Extended Release |
| Active Ingredient(s): | 500 mg/1 & nbsp; Metformin Hydrochloride Extended Release |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metformin Hydrochloride Extended Release
| Product NDC: | 49349-201 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075979 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110421 |
Package Information of Metformin Hydrochloride Extended Release
| Package NDC: | 49349-201-02 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-201-02) |
NDC Information of Metformin Hydrochloride Extended Release
| NDC Code | 49349-201-02 |
| Proprietary Name | Metformin Hydrochloride Extended Release |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-201-02) |
| Product NDC | 49349-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metformin Hydrochloride Extended Release |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110421 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
