Glimepiride 61442-0117
Product NDC
61442-0117- Manufacturer
- Carlsbad Technology, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA077911
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Glimepiride | 4 mg/1 |
Drug Class
Sulfonylurea [EPC]Sulfonylurea Compounds [CS]Sulfonylurea [EPC]
Packaging Options(3)
100 TABLET in 1 BOTTLE (61442-117-01)
500 TABLET in 1 BOTTLE (61442-117-05)
1000 TABLET in 1 BOTTLE (61442-117-10)