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GLIPIZIDE and METFORMIN HYDROCHLORIDE
GLIPIZIDE and METFORMIN HYDROCHLORIDE - 60760-175-30 - (GLIPIZIDE and METFORMIN HYDROCHLORIDE)
Drug Information of GLIPIZIDE and METFORMIN HYDROCHLORIDE
| Product NDC: | 60760-175 |
| Proprietary Name: | GLIPIZIDE and METFORMIN HYDROCHLORIDE |
| Non Proprietary Name: | GLIPIZIDE and METFORMIN HYDROCHLORIDE |
| Active Ingredient(s): | 2.5; 500 mg/1; mg/1 & nbsp; GLIPIZIDE and METFORMIN HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GLIPIZIDE and METFORMIN HYDROCHLORIDE
| Product NDC: | 60760-175 |
| Labeler Name: | St Marys Medical Park Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077270 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130509 |
Package Information of GLIPIZIDE and METFORMIN HYDROCHLORIDE
| Package NDC: | 60760-175-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-175-30) |
NDC Information of GLIPIZIDE and METFORMIN HYDROCHLORIDE
| NDC Code | 60760-175-30 |
| Proprietary Name | GLIPIZIDE and METFORMIN HYDROCHLORIDE |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-175-30) |
| Product NDC | 60760-175 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GLIPIZIDE and METFORMIN HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130509 |
| Marketing Category Name | ANDA |
| Labeler Name | St Marys Medical Park Pharmacy |
| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
| Strength Number | 2.5; 500 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
