NDC 71610-151 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC71610-151

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 · ANDA078413
Marketed since
May 4, 2007
Listing expires
December 31, 2026
Pharmacologic class
gamma-Aminobutyric Acid-ergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for zolpidem tartrate →

Package NDC codes (7)

Package NDCDescriptionSince
71610-151-1515 TABLET, FILM COATED in 1 BOTTLE (71610-151-15)Sep 18, 2018
71610-151-2020 TABLET, FILM COATED in 1 BOTTLE (71610-151-20)Sep 18, 2018
71610-151-2828 TABLET, FILM COATED in 1 BOTTLE (71610-151-28)Sep 18, 2018
71610-151-3030 TABLET, FILM COATED in 1 BOTTLE (71610-151-30)Sep 18, 2018
71610-151-4545 TABLET, FILM COATED in 1 BOTTLE (71610-151-45)Sep 18, 2018
71610-151-5360 TABLET, FILM COATED in 1 BOTTLE (71610-151-53)Sep 18, 2018
71610-151-6090 TABLET, FILM COATED in 1 BOTTLE (71610-151-60)Sep 18, 2018

Other zolpidem tartrate products