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Zolpidem Tartrate

NDC 47335-307 · Sun Pharmaceutical Industries, Inc.

Generic nameZolpidem Tartrate
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)ZOLPIDEM TARTRATE
Strength6.25 mg/1
Pharmacologic classCentral Nervous System Depression [PE], GABA A Agonists [MoA], Pyridines [CS], gamma-Aminobutyric Acid-ergic Agonist [EPC]
DEA scheduleCIV
Marketing categoryANDA

Packages

47335-307-13 — 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-307-13)

47335-307-88 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-307-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 47335-308 — Zolpidem Tartrate, 49884-898 — Zolpidem tartrate sublingual, 49884-899 — Zolpidem tartrate sublingual, 50090-1022 — zolpidem tartrate, 50090-2649 — Zolpidem Tartrate, 50090-3878 — Zolpidem Tartrate, 50090-3879 — Zolpidem Tartrate, 50090-5095 — Zolpidem Tartrate, 50090-5804 — zolpidem tartrate, 50090-6070 — 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.