NDC 71610-770 – Zolpidem Tartrate

Zolpidem Tartrate 6.25 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71610-770

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem tartrate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021774
Marketed since
October 14, 2010
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 (5)

Package NDCDescriptionSince
71610-770-1515 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-15)Jan 19, 2024
71610-770-2828 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-28)Jan 19, 2024
71610-770-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-30)Jan 19, 2024
71610-770-5360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-53)Jan 19, 2024
71610-770-6090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-60)Jan 19, 2024

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