NDC 71610-152 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC71610-152

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 (6)

Package NDCDescriptionSince
71610-152-1010 TABLET, FILM COATED in 1 BOTTLE (71610-152-10)Sep 18, 2018
71610-152-1515 TABLET, FILM COATED in 1 BOTTLE (71610-152-15)Sep 18, 2018
71610-152-2020 TABLET, FILM COATED in 1 BOTTLE (71610-152-20)Sep 18, 2018
71610-152-2121 TABLET, FILM COATED in 1 BOTTLE (71610-152-21)Sep 18, 2018
71610-152-2828 TABLET, FILM COATED in 1 BOTTLE (71610-152-28)Sep 18, 2018
71610-152-3030 TABLET, FILM COATED in 1 BOTTLE (71610-152-30)Sep 18, 2018

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