Glipizide 68788-8487
Product NDC
68788-8487- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 19, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA204720
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Glipizide | 2.5 mg/1 |
Drug Class
Sulfonylurea [EPC]Sulfonylurea Compounds [CS]Sulfonylurea [EPC]
Packaging Options(4)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-1)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-3)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-6)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-9)