NDC 70771-1016 – Nateglinide
Nateglinide 120 mg/1 · Tablet, Film Coated · Oral
Product NDC70771-1016
Product details
- Brand name
- Nateglinide
- Generic name
- Nateglinide
- Labeler
- Zydus Lifesciences Limited
- 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 120 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1016-0 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1016-0) | Oct 27, 2016 |
| 70771-1016-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1016-1) | Oct 27, 2016 |
| 70771-1016-3 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1016-3) | Oct 27, 2016 |
| 70771-1016-4 | 10 BLISTER PACK in 1 CARTON (70771-1016-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1016-2) | Oct 27, 2016 |
| 70771-1016-5 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1016-5) | Oct 27, 2016 |
| 70771-1016-9 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1016-9) | Oct 27, 2016 |
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