Zolpidem Tartrate

NDC 60760-761 · ST. MARY'S MEDICAL PARK PHARMACY

Generic nameZolpidem Tartrate

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)ZOLPIDEM TARTRATE

Strength5 mg/1

Pharmacologic classCentral Nervous System Depression [PE], GABA A Receptor Positive Modulators [MoA], gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]

DEA scheduleCIV

Marketing categoryANDA

Packages

60760-761-30 — 30 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-761-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-942 — zolpidem tartrate, 51991-981 — Zolpidem Tartrate, 51991-982 — Zolpidem Tartrate, 52427-775 — zolpidem tartrate, 55154-1398 — zolpidem tartrate, 55700-357 — zolpidem tartrate, 60290-089 — Zolpidem Tartrate, 60687-838 — Zolpidem Tartrate, 60760-288 — zolpidem tartrate, 60760-515 — zolpidem tartrate, 60760-819 — Zolpidem Tartrate, 61919-663 — ZOLPIDEM TARTRATE, 61919-751 — ZOLPIDEM TARTRATE, 62135-778 — Zolpidem Tartrate, 62135-779 — Zolpidem Tartrate, 63187-114 — Zolpidem tartrate, 63187-558 — zolpidem tartrate, 63187-565 — zolpidem tartrate, 63187-682 — Zolpidem Tartrate, 63187-690 — Zolpidem Tartrate, +124 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.