NDC 16714-621 – Zolpidem Tartrate
Zolpidem Tartrate 5 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-621
Product details
- Brand name
- Zolpidem Tartrate
- Generic name
- Zolpidem Tartrate
- Labeler
- NorthStar Rx 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 5 mg/1
Uses, dosage, side effects and warnings for zolpidem tartrate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 16714-621-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-621-01) | May 4, 2007 |
| 16714-621-02 | 500 TABLET, FILM COATED in 1 BOTTLE (16714-621-02) | May 4, 2007 |
| 16714-621-11 | 10 BLISTER PACK in 1 CARTON (16714-621-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-621-10) | May 4, 2007 |
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