NDC 16729-003 – Glimepiride
Glimepiride 4 mg/1 · Tablet · Oral
Product NDC16729-003
Product details
- Brand name
- Glimepiride
- Generic name
- Glimepiride
- Labeler
- Accord Healthcare Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078181
- Marketed since
- August 23, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sulfonylurea
Active ingredients
- Glimepiride 4 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16729-003-01 | 100 TABLET in 1 BOTTLE (16729-003-01) | Aug 23, 2007 |
| 16729-003-16 | 500 TABLET in 1 BOTTLE (16729-003-16) | Aug 25, 2016 |
Recalls mentioning this NDC
- D-0393-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0394-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0395-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection.
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