NDC 71335-0116 – Eszopiclone
Eszopiclone 3 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0116
Product details
- Brand name
- Eszopiclone
- Generic name
- Eszopiclone
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202929
- Marketed since
- April 25, 2014
- Listing expires
- December 31, 2026
Active ingredients
- Eszopiclone 3 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0116-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0116-1) | Jan 24, 2017 |
| 71335-0116-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0116-2) | Jan 24, 2017 |
| 71335-0116-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0116-3) | Jan 24, 2017 |
| 71335-0116-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0116-4) | Jan 24, 2017 |
| 71335-0116-5 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0116-5) | Jan 24, 2017 |
| 71335-0116-6 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0116-6) | Jan 24, 2017 |
| 71335-0116-7 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0116-7) | Jan 24, 2017 |
| 71335-0116-8 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0116-8) | Jan 24, 2017 |
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