ZOLPIDEM TARTRATE

NDC 68071-4598 · NuCare Pharmaceuticals,Inc.

Generic namezolpidem tartrate

Dosage formTABLET

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

68071-4598-3 — 30 TABLET in 1 BOTTLE (68071-4598-3)

68071-4598-4 — 14 TABLET in 1 BOTTLE (68071-4598-4)

68071-4598-5 — 45 TABLET in 1 BOTTLE (68071-4598-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-8998 — Zolpidem Tartrate, 63629-8999 — Zolpidem Tartrate, 63629-9613 — Zolpidem Tartrate, 63629-9614 — Zolpidem Tartrate, 65862-159 — Zolpidem Tartrate, 65862-160 — Zolpidem Tartrate, 68071-1887 — zolpidem tartrate, 68071-2232 — zolpidem tartrate, 68071-2354 — Zolpidem Tartrate, 68071-3770 — Zolpidem Tartrate, 68071-5063 — zolpidem tartrate, 68071-5093 — zolpidem tartrate, 68071-5120 — zolpidem tartrate, 68180-779 — Zolpidem Tartrate, 68180-780 — Zolpidem Tartrate, 68788-7422 — Zolpidem Tartrate, 68788-8376 — Zolpidem Tartrate, 68788-8654 — Zolpidem Tartrate, 68788-8854 — Zolpidem Tartrate, 68788-9126 — 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.