NDC 71610-192 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC71610-192

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
71610-192-1515 TABLET, FILM COATED in 1 BOTTLE (71610-192-15)Nov 8, 2018
71610-192-2020 TABLET, FILM COATED in 1 BOTTLE (71610-192-20)Nov 8, 2018
71610-192-2525 TABLET, FILM COATED in 1 BOTTLE (71610-192-25)Nov 8, 2018
71610-192-2828 TABLET, FILM COATED in 1 BOTTLE (71610-192-28)Nov 8, 2018
71610-192-3030 TABLET, FILM COATED in 1 BOTTLE (71610-192-30)Nov 8, 2018
71610-192-5922 TABLET, FILM COATED in 1 BOTTLE (71610-192-59)Nov 8, 2018
71610-192-6090 TABLET, FILM COATED in 1 BOTTLE (71610-192-60)Nov 8, 2018

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