NDC 50090-2649 – Zolpidem Tartrate

Zolpidem Tartrate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC50090-2649

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078413
Marketed since
May 4, 2007
Listing expires
December 31, 2027
Pharmacologic class
gamma-Aminobutyric Acid A Receptor Positive Modulator

Active ingredients

Uses, dosage, side effects and warnings for zolpidem tartrate →

Package NDC codes (4)

Package NDCDescriptionSince
50090-2649-020 TABLET, FILM COATED in 1 BOTTLE (50090-2649-0)Dec 20, 2016
50090-2649-130 TABLET, FILM COATED in 1 BOTTLE (50090-2649-1)Jan 17, 2017
50090-2649-33 TABLET, FILM COATED in 1 BOTTLE (50090-2649-3)Nov 28, 2016
50090-2649-460 TABLET, FILM COATED in 1 BOTTLE (50090-2649-4)Nov 15, 2024

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