NDC 71335-9629 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC71335-9629

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA077322
Marketed since
April 23, 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
71335-9629-025 TABLET, COATED in 1 BOTTLE (71335-9629-0)Jan 23, 2023
71335-9629-130 TABLET, COATED in 1 BOTTLE (71335-9629-1)Jan 23, 2023
71335-9629-260 TABLET, COATED in 1 BOTTLE (71335-9629-2)Jan 23, 2023
71335-9629-310 TABLET, COATED in 1 BOTTLE (71335-9629-3)Jan 23, 2023
71335-9629-4100 TABLET, COATED in 1 BOTTLE (71335-9629-4)Jan 23, 2023
71335-9629-520 TABLET, COATED in 1 BOTTLE (71335-9629-5)Jan 23, 2023
71335-9629-690 TABLET, COATED in 1 BOTTLE (71335-9629-6)Jan 23, 2023
71335-9629-756 TABLET, COATED in 1 BOTTLE (71335-9629-7)Jan 23, 2023
71335-9629-828 TABLET, COATED in 1 BOTTLE (71335-9629-8)Jan 23, 2023
71335-9629-9120 TABLET, COATED in 1 BOTTLE (71335-9629-9)Jan 23, 2023

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