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Glucotrol
Glucotrol - 0049-1620-30 - (GLIPIZIDE)
Drug Information of Glucotrol
| Product NDC: | 0049-1620 |
| Proprietary Name: | Glucotrol |
| Non Proprietary Name: | GLIPIZIDE |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; GLIPIZIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glucotrol
| Product NDC: | 0049-1620 |
| Labeler Name: | Roerig |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020329 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19940426 |
Package Information of Glucotrol
| Package NDC: | 0049-1620-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0049-1620-30) |
NDC Information of Glucotrol
| NDC Code | 0049-1620-30 |
| Proprietary Name | Glucotrol |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0049-1620-30) |
| Product NDC | 0049-1620 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GLIPIZIDE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19940426 |
| Marketing Category Name | NDA |
| Labeler Name | Roerig |
| Substance Name | GLIPIZIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
