NDC 71335-0180 – Glimepiride
Glimepiride 4 mg/1 · Tablet · Oral
Product NDC71335-0180
Product details
- Brand name
- Glimepiride
- Generic name
- Glimepiride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078181
- Marketed since
- August 23, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- Sulfonylurea
Active ingredients
- Glimepiride 4 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0180-1 | 30 TABLET in 1 BOTTLE (71335-0180-1) | Dec 19, 2014 |
| 71335-0180-2 | 60 TABLET in 1 BOTTLE (71335-0180-2) | Dec 19, 2014 |
| 71335-0180-3 | 90 TABLET in 1 BOTTLE (71335-0180-3) | Dec 19, 2014 |
| 71335-0180-4 | 180 TABLET in 1 BOTTLE (71335-0180-4) | Dec 19, 2014 |
| 71335-0180-5 | 100 TABLET in 1 BOTTLE (71335-0180-5) | Apr 5, 2024 |
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