NDC 68382-721 – Nateglinide
Nateglinide 60 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-721
Product details
- Brand name
- Nateglinide
- Generic name
- Nateglinide
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205248
- Marketed since
- October 27, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Glinide
Active ingredients
- Nateglinide 60 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-721-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-721-01) | Oct 27, 2016 |
| 68382-721-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-721-05) | Oct 27, 2016 |
| 68382-721-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-721-06) | Oct 27, 2016 |
| 68382-721-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-721-10) | Oct 27, 2016 |
| 68382-721-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-721-16) | Oct 27, 2016 |
| 68382-721-77 | 10 BLISTER PACK in 1 CARTON (68382-721-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Oct 27, 2016 |
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