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Zolpidem tartrate sublingual

NDC 49884-898 · Par Health USA, LLC

Generic nameZolpidem tartrate sublingual
Dosage formTABLET
RouteSUBLINGUAL
Active ingredient(s)ZOLPIDEM TARTRATE
Strength1.75 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

49884-898-11 — 30 POUCH in 1 CARTON (49884-898-11) / 1 TABLET in 1 POUCH (49884-898-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 47335-307 — Zolpidem Tartrate, 47335-308 — Zolpidem Tartrate, 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, 50090-7434 — Zolpidem Tartrate, 51407-761 — 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.