NDC 0781-5317 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC0781-5317

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Sandoz Inc
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA077322
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 (4)

Package NDCDescriptionSince
0781-5317-01100 TABLET, COATED in 1 BOTTLE (0781-5317-01)Apr 23, 2007
0781-5317-05500 TABLET, COATED in 1 BOTTLE (0781-5317-05)Apr 23, 2007
0781-5317-101000 TABLET, COATED in 1 BOTTLE (0781-5317-10)Apr 23, 2007
0781-5317-3130 TABLET, COATED in 1 BOTTLE (0781-5317-31)Apr 23, 2007

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