Glipizide - glipizide
Navigation: NDC > Supplier starting with: G > GREENSTONE LLC| Field | Value |
|---|---|
| NDC Code: | 59762-5031 |
| Proprietary Name: | Glipizide |
| Suffix: | XL |
| Non-Proprietary Name: | glipizide |
| Dosage Form: | TABLET, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 11-06-2004 |
| End of Marketing: | 30-06-2014 |
| Category Name: | NDA AUTHORIZED GENERIC |
| Application Number: | NDA020329 |
| Labeler: | GREENSTONE LLC |
| Substance Name: | GLIPIZIDE |
| Active Numerator Strength: | 2.5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
| DEA Schedule: |