NDC 71610-904 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC71610-904

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 (9)

Package NDCDescriptionSince
71610-904-1010 TABLET, FILM COATED in 1 BOTTLE (71610-904-10)May 6, 2025
71610-904-1414 TABLET, FILM COATED in 1 BOTTLE (71610-904-14)May 6, 2025
71610-904-1515 TABLET, FILM COATED in 1 BOTTLE (71610-904-15)May 6, 2025
71610-904-2020 TABLET, FILM COATED in 1 BOTTLE (71610-904-20)May 13, 2025
71610-904-2828 TABLET, FILM COATED in 1 BOTTLE (71610-904-28)May 6, 2025
71610-904-3030 TABLET, FILM COATED in 1 BOTTLE (71610-904-30)May 6, 2025
71610-904-4545 TABLET, FILM COATED in 1 BOTTLE (71610-904-45)May 6, 2025
71610-904-5360 TABLET, FILM COATED in 1 BOTTLE (71610-904-53)May 6, 2025
71610-904-6090 TABLET, FILM COATED in 1 BOTTLE (71610-904-60)May 6, 2025

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