NDC 72789-323 – Zolpidem Tartrate

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

Human Prescription Drug DEA schedule CIV

Product NDC72789-323

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
PD-Rx Pharmaceuticals, Inc.
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 A Receptor Positive Modulator

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
72789-323-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-01)May 4, 2007
72789-323-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-10)Oct 30, 2023
72789-323-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-14)Jan 10, 2024
72789-323-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-15)Sep 25, 2023
72789-323-2121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-21)Nov 9, 2023
72789-323-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-30)May 4, 2007
72789-323-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-60)May 4, 2007

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