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Metformin hydrochloride
Metformin hydrochloride - 55154-1676-9 - (Metformin hydrochloride)
Drug Information of Metformin hydrochloride
| Product NDC: | 55154-1676 |
| Proprietary Name: | Metformin hydrochloride |
| Non Proprietary Name: | Metformin hydrochloride |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Metformin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metformin hydrochloride
| Product NDC: | 55154-1676 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079148 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090603 |
Package Information of Metformin hydrochloride
| Package NDC: | 55154-1676-9 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (55154-1676-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Metformin hydrochloride
| NDC Code | 55154-1676-9 |
| Proprietary Name | Metformin hydrochloride |
| Package Description | 6 BLISTER PACK in 1 CARTON (55154-1676-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 55154-1676 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metformin hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090603 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
