NDC 76420-416 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC76420-416

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Asclemed USA, 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 (6)

Package NDCDescriptionSince
76420-416-001000 TABLET, FILM COATED in 1 BOTTLE (76420-416-00)Jul 24, 2025
76420-416-01100 TABLET, FILM COATED in 1 BOTTLE (76420-416-01)Jul 24, 2025
76420-416-05500 TABLET, FILM COATED in 1 BOTTLE (76420-416-05)Jul 24, 2025
76420-416-3030 TABLET, FILM COATED in 1 BOTTLE (76420-416-30)Jul 24, 2025
76420-416-6060 TABLET, FILM COATED in 1 BOTTLE (76420-416-60)Jul 24, 2025
76420-416-9090 TABLET, FILM COATED in 1 BOTTLE (76420-416-90)Jul 24, 2025

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