NDC 72789-323 – Zolpidem Tartrate
Zolpidem Tartrate 10 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-323
Product details
- Brand name
- Zolpidem Tartrate
- Generic name
- Zolpidem Tartrate
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- 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 A Receptor Positive Modulator
Active ingredients
- Zolpidem Tartrate 10 mg/1
Uses, dosage, side effects and warnings for zolpidem tartrate →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 72789-323-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-01) | May 4, 2007 |
| 72789-323-10 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-10) | Oct 30, 2023 |
| 72789-323-14 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-14) | Jan 10, 2024 |
| 72789-323-15 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-15) | Sep 25, 2023 |
| 72789-323-21 | 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-21) | Nov 9, 2023 |
| 72789-323-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-30) | May 4, 2007 |
| 72789-323-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-60) | May 4, 2007 |
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