NDC 55111-320 – Glimepiride
Glimepiride 1 mg/1 · Tablet · Oral
Product NDC55111-320
Product details
- Brand name
- Glimepiride
- Generic name
- Glimepiride
- Labeler
- Dr. Reddy's Laboratories Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077091
- Marketed since
- October 6, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sulfonylurea
Active ingredients
- Glimepiride 1 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 55111-320-01 | 100 TABLET in 1 BOTTLE (55111-320-01) | Oct 6, 2005 |
| 55111-320-05 | 500 TABLET in 1 BOTTLE (55111-320-05) | Oct 6, 2005 |
| 55111-320-30 | 30 TABLET in 1 BOTTLE (55111-320-30) | Oct 6, 2005 |
| 55111-320-78 | 100 BLISTER PACK in 1 CARTON (55111-320-78) / 1 TABLET in 1 BLISTER PACK (55111-320-79) | Oct 6, 2005 |
Recalls mentioning this NDC
- D-0312-2024 Feb 14, 2024 · Class III
Misprint on tablet - D-0313-2024 Feb 14, 2024 · Class III
Misprint on tablet
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