NDC 71610-915 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC71610-915

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem tartrate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077214
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 (13)

Package NDCDescriptionSince
71610-915-1010 TABLET, FILM COATED in 1 BOTTLE (71610-915-10)Jun 23, 2025
71610-915-1414 TABLET, FILM COATED in 1 BOTTLE (71610-915-14)Jun 23, 2025
71610-915-1515 TABLET, FILM COATED in 1 BOTTLE (71610-915-15)Jun 23, 2025
71610-915-2020 TABLET, FILM COATED in 1 BOTTLE (71610-915-20)Jun 23, 2025
71610-915-2121 TABLET, FILM COATED in 1 BOTTLE (71610-915-21)Jun 23, 2025
71610-915-2525 TABLET, FILM COATED in 1 BOTTLE (71610-915-25)Jun 23, 2025
71610-915-2828 TABLET, FILM COATED in 1 BOTTLE (71610-915-28)Jun 23, 2025
71610-915-3030 TABLET, FILM COATED in 1 BOTTLE (71610-915-30)Jun 23, 2025
71610-915-4545 TABLET, FILM COATED in 1 BOTTLE (71610-915-45)Jun 23, 2025
71610-915-5360 TABLET, FILM COATED in 1 BOTTLE (71610-915-53)Jun 23, 2025
71610-915-5922 TABLET, FILM COATED in 1 BOTTLE (71610-915-59)Jun 23, 2025
71610-915-6090 TABLET, FILM COATED in 1 BOTTLE (71610-915-60)Jun 23, 2025
71610-915-6211 TABLET, FILM COATED in 1 BOTTLE (71610-915-62)Jun 23, 2025

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