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Metformin hydrochloride
Metformin hydrochloride - 67877-159-10 - (Metformin hydrochloride)
Drug Information of Metformin hydrochloride
| Product NDC: | 67877-159 |
| 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: | 67877-159 |
| Labeler Name: | Ascend Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201991 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130301 |
Package Information of Metformin hydrochloride
| Package NDC: | 67877-159-10 |
| Package Description: | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-159-10) |
NDC Information of Metformin hydrochloride
| NDC Code | 67877-159-10 |
| Proprietary Name | Metformin hydrochloride |
| Package Description | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-159-10) |
| Product NDC | 67877-159 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metformin hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | ANDA |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
