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GLIPIZIDE
GLIPIZIDE - 49349-092-02 - (GLIPIZIDE)
Drug Information of GLIPIZIDE
| Product NDC: | 49349-092 |
| Proprietary Name: | GLIPIZIDE |
| Non Proprietary Name: | GLIPIZIDE |
| Active Ingredient(s): | 5 mg/1 & nbsp; GLIPIZIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GLIPIZIDE
| Product NDC: | 49349-092 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074223 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101123 |
Package Information of GLIPIZIDE
| Package NDC: | 49349-092-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-092-02) |
NDC Information of GLIPIZIDE
| NDC Code | 49349-092-02 |
| Proprietary Name | GLIPIZIDE |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-092-02) |
| Product NDC | 49349-092 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GLIPIZIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101123 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | GLIPIZIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
