NDC 71610-192 – Zolpidem Tartrate
Zolpidem Tartrate 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71610-192
Product details
- Brand name
- Zolpidem Tartrate
- Generic name
- Zolpidem Tartrate
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078413
- Marketed since
- May 4, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- gamma-Aminobutyric Acid-ergic Agonist
Active ingredients
- Zolpidem Tartrate 10 mg/1
Uses, dosage, side effects and warnings for Zolpidem tartrate →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71610-192-15 | 15 TABLET, FILM COATED in 1 BOTTLE (71610-192-15) | Nov 8, 2018 |
| 71610-192-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71610-192-20) | Nov 8, 2018 |
| 71610-192-25 | 25 TABLET, FILM COATED in 1 BOTTLE (71610-192-25) | Nov 8, 2018 |
| 71610-192-28 | 28 TABLET, FILM COATED in 1 BOTTLE (71610-192-28) | Nov 8, 2018 |
| 71610-192-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-192-30) | Nov 8, 2018 |
| 71610-192-59 | 22 TABLET, FILM COATED in 1 BOTTLE (71610-192-59) | Nov 8, 2018 |
| 71610-192-60 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-192-60) | Nov 8, 2018 |
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