NDC 72722-103 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC72722-103

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem tartrate
Labeler
The ACME Laboratories Ltd.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077214
Marketed since
September 24, 2020
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 (3)

Package NDCDescriptionSince
72722-103-0130 TABLET, FILM COATED in 1 BOTTLE (72722-103-01)Nov 30, 2024
72722-103-05100 TABLET, FILM COATED in 1 BOTTLE (72722-103-05)Nov 30, 2024
72722-103-071000 TABLET, FILM COATED in 1 BOTTLE (72722-103-07)Nov 30, 2024

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