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Metformin hydrochloride
Metformin hydrochloride - 49252-001-17 - (Metformin hydrochloride)
Drug Information of Metformin hydrochloride
| Product NDC: | 49252-001 |
| 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: | 49252-001 |
| Labeler Name: | Inventia Healthcare Private Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201991 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120601 |
Package Information of Metformin hydrochloride
| Package NDC: | 49252-001-17 |
| Package Description: | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (49252-001-17) |
NDC Information of Metformin hydrochloride
| NDC Code | 49252-001-17 |
| Proprietary Name | Metformin hydrochloride |
| Package Description | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (49252-001-17) |
| Product NDC | 49252-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metformin hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | ANDA |
| Labeler Name | Inventia Healthcare Private Limited |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
