NDC 50090-3879 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC50090-3879

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, 2026
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
50090-3879-020 TABLET, FILM COATED in 1 BOTTLE (50090-3879-0)Nov 28, 2018
50090-3879-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3879-1)Nov 28, 2014
50090-3879-33 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3879-3)Nov 28, 2014
50090-3879-460 TABLET, FILM COATED in 1 BOTTLE (50090-3879-4)Nov 28, 2018

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