NDC 68788-7667 – Eszopiclone
Eszopiclone 1 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-7667
Product details
- Brand name
- Eszopiclone
- Generic name
- Eszopiclone
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208451
- Marketed since
- February 28, 2020
- Listing expires
- December 31, 2027
Active ingredients
- Eszopiclone 1 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7667-0 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7667-0) | Feb 28, 2020 |
| 68788-7667-1 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-7667-1) | Feb 28, 2020 |
| 68788-7667-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7667-2) | Feb 28, 2020 |
| 68788-7667-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7667-3) | Feb 28, 2020 |
| 68788-7667-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-7667-5) | Feb 28, 2020 |
| 68788-7667-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7667-6) | Feb 28, 2020 |
| 68788-7667-7 | 7 TABLET, FILM COATED in 1 BOTTLE (68788-7667-7) | Feb 28, 2020 |
| 68788-7667-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7667-9) | Feb 28, 2020 |
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