NDC 42571-103 – Glimepiride
Glimepiride 4 mg/1 · Tablet · Oral
Product NDC42571-103
Product details
- Brand name
- Glimepiride
- Generic name
- Glimepiride
- Labeler
- Micro Labs Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091220
- Marketed since
- June 13, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sulfonylurea
Active ingredients
- Glimepiride 4 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 42571-103-01 | 100 TABLET in 1 BOTTLE (42571-103-01) | Jun 13, 2013 |
| 42571-103-05 | 500 TABLET in 1 BOTTLE (42571-103-05) | Jun 13, 2013 |
Recalls mentioning this NDC
- D-0046-2015 Nov 5, 2014 · Class II
Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.
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