Ambien

NDC 0024-5421 · Sanofi-Aventis U.S. LLC

Generic namezolpidem tartrate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ZOLPIDEM TARTRATE

Strength10 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 categoryNDA

Packages

0024-5421-31 — 100 TABLET, FILM COATED in 1 BOTTLE (0024-5421-31)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0024-5401 — zolpidem tartrate, 0037-6010 — Zolpidem Tartrate, 0037-6050 — Zolpidem Tartrate, 0713-5401 — zolpidem tartrate, 0713-5421 — zolpidem tartrate, 0713-5501 — zolpidem tartrate, 0713-5521 — zolpidem tartrate, 0781-5315 — Zolpidem tartrate, 0781-5316 — Zolpidem tartrate, 0781-5317 — Zolpidem Tartrate, 0781-5318 — Zolpidem Tartrate, 0904-6082 — zolpidem tartrate, 13668-007 — zolpidem tartrate, 13668-008 — zolpidem tartrate, 13668-775 — Zolpidem Tartrate, 16714-621 — Zolpidem Tartrate, 16714-622 — Zolpidem Tartrate, 17224-970 — ZOLPIDEM TARTRATE, 43386-761 — zolpidem tartrate, 43386-762 — 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.