NDC 71335-0154 – Zolpidem Tartrate

Zolpidem Tartrate 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0154

Product details

Brand name
Zolpidem Tartrate
Generic name
zolpidem tartrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077903
Marketed since
September 5, 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 (10)

Package NDCDescriptionSince
71335-0154-05 TABLET in 1 BOTTLE (71335-0154-0)May 29, 2024
71335-0154-130 TABLET in 1 BOTTLE (71335-0154-1)Apr 4, 2018
71335-0154-260 TABLET in 1 BOTTLE (71335-0154-2)Feb 22, 2018
71335-0154-3100 TABLET in 1 BOTTLE (71335-0154-3)Aug 31, 2023
71335-0154-450 TABLET in 1 BOTTLE (71335-0154-4)May 29, 2024
71335-0154-590 TABLET in 1 BOTTLE (71335-0154-5)Feb 14, 2018
71335-0154-610 TABLET in 1 BOTTLE (71335-0154-6)May 11, 2018
71335-0154-715 TABLET in 1 BOTTLE (71335-0154-7)Feb 27, 2018
71335-0154-828 TABLET in 1 BOTTLE (71335-0154-8)Jul 11, 2018
71335-0154-9120 TABLET in 1 BOTTLE (71335-0154-9)Oct 3, 2018

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