ZOLPIDEM TARTRATE

NDC 72722-103 · The ACME Laboratories Ltd.

Generic namezolpidem tartrate

Dosage formTABLET, FILM 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

72722-103-01 — 30 TABLET, FILM COATED in 1 BOTTLE (72722-103-01)

72722-103-05 — 100 TABLET, FILM COATED in 1 BOTTLE (72722-103-05)

72722-103-07 — 1000 TABLET, FILM COATED in 1 BOTTLE (72722-103-07)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-839 — Zolpidem Tartrate, 71610-847 — Zolpidem Tartrate, 71610-848 — Zolpidem Tartrate, 71610-904 — zolpidem tartrate, 71610-913 — Zolpidem Tartrate, 71610-915 — zolpidem tartrate, 72162-1982 — Zolpidem Tartrate, 72162-1983 — Zolpidem Tartrate, 72162-2441 — Zolpidem Tartrate, 72189-230 — ZOLPIDEM TARTRATE, 72722-104 — zolpidem tartrate, 72789-323 — Zolpidem Tartrate, 72789-390 — Zolpidem Tartrate, 76420-233 — zolpidem tartrate, 76420-263 — zolpidem tartrate, 76420-318 — Zolpidem Tartrate, 76420-319 — Zolpidem Tartrate, 76420-416 — Zolpidem Tartrate, 76420-417 — Zolpidem Tartrate, 76420-494 — 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.