NDC 60687-838 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC60687-838

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078413
Marketed since
September 1, 2024
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 (1)

Package NDCDescriptionSince
60687-838-01100 BLISTER PACK in 1 CARTON (60687-838-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-838-11)Sep 1, 2024

Other Zolpidem tartrate products