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Zolpidem Tartrate

NDC 16714-622 · NorthStar Rx 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 Agonists [MoA], Pyridines [CS], gamma-Aminobutyric Acid-ergic Agonist [EPC]
DEA scheduleCIV
Marketing categoryANDA

Packages

16714-622-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16714-622-01)

16714-622-02 — 500 TABLET, FILM COATED in 1 BOTTLE (16714-622-02)

16714-622-11 — 10 BLISTER PACK in 1 CARTON (16714-622-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-622-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 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, 50090-2649 — Zolpidem Tartrate, 50090-3878 — 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.