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Glipizide
Glipizide - 21695-470-78 - (Glipizide)
Drug Information of Glipizide
| Product NDC: | 21695-470 |
| Proprietary Name: | Glipizide |
| Non Proprietary Name: | Glipizide |
| Active Ingredient(s): | 10 mg/1 & nbsp; Glipizide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glipizide
| Product NDC: | 21695-470 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074223 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950227 |
Package Information of Glipizide
| Package NDC: | 21695-470-78 |
| Package Description: | 180 TABLET in 1 BOTTLE (21695-470-78) |
NDC Information of Glipizide
| NDC Code | 21695-470-78 |
| Proprietary Name | Glipizide |
| Package Description | 180 TABLET in 1 BOTTLE (21695-470-78) |
| Product NDC | 21695-470 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Glipizide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19950227 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | GLIPIZIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
