Glipizide 72789-0130
Product NDC
72789-0130- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 25, 2002
- Listing Expires
- December 31, 2027
- Application
- ANDA075795
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Glipizide | 5 mg/1 |
Drug Class
Sulfonylurea [EPC]Sulfonylurea Compounds [CS]Sulfonylurea [EPC]
Packaging Options(2)
30 TABLET in 1 BOTTLE, PLASTIC (72789-130-30)
90 TABLET in 1 BOTTLE, PLASTIC (72789-130-90)