NDC 68071-3770 – Zolpidem Tartrate

Zolpidem Tartrate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC68071-3770

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
NuCare 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

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

Package NDC codes (1)

Package NDCDescriptionSince
68071-3770-990 TABLET, FILM COATED in 1 BOTTLE (68071-3770-9)Jan 13, 2025

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