Glipizide 82868-0035
Product NDC
82868-0035- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 9, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA206928
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Glipizide | 10 mg/1 |
Drug Class
Sulfonylurea [EPC]Sulfonylurea Compounds [CS]Sulfonylurea [EPC]
Packaging Options(2)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-035-30)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-035-90)