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Zolpidem Tartrate

NDC 50090-2649 · A-S Medication Solutions

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

50090-2649-0 — 20 TABLET, FILM COATED in 1 BOTTLE (50090-2649-0)

50090-2649-1 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-2649-1)

50090-2649-3 — 3 TABLET, FILM COATED in 1 BOTTLE (50090-2649-3)

50090-2649-4 — 60 TABLET, FILM COATED in 1 BOTTLE (50090-2649-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-621 — Zolpidem Tartrate, 16714-622 — Zolpidem Tartrate, 17224-970 — ZOLPIDEM TARTRATE, 43386-761 — zolpidem tartrate, 43386-762 — zolpidem tartrate, 47335-307 — Zolpidem Tartrate, 47335-308 — Zolpidem Tartrate, 49884-898 — Zolpidem tartrate sublingual, 49884-899 — Zolpidem tartrate sublingual, 50090-1022 — zolpidem tartrate, 50090-3878 — Zolpidem Tartrate, 50090-3879 — Zolpidem Tartrate, 50090-5095 — Zolpidem Tartrate, 50090-5804 — zolpidem tartrate, 50090-6070 — Zolpidem Tartrate, 50090-7434 — Zolpidem Tartrate, 51407-761 — zolpidem tartrate, 51407-762 — zolpidem tartrate, 51407-877 — Zolpidem Tartrate, 51407-878 — Zolpidem Tartrate, +124 more

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