Glimepiride 71921-0216
Product NDC
71921-0216- Manufacturer
- Florida Pharmaceutical Products, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 31, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA202112
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Glimepiride | 4 mg/1 |
Drug Class
Sulfonylurea [EPC]Sulfonylurea Compounds [CS]Sulfonylurea [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (71921-216-01)
500 TABLET in 1 BOTTLE (71921-216-50)