ZOLPIDEM TARTRATE

NDC 68180-780 · Lupin Pharmaceuticals, Inc.

Generic nameZolpidem Tartrate

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)ZOLPIDEM TARTRATE

Strength12.5 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

68180-780-04 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-780-04)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-160 — Zolpidem Tartrate, 68071-1887 — zolpidem tartrate, 68071-2232 — zolpidem tartrate, 68071-2354 — Zolpidem Tartrate, 68071-3770 — Zolpidem Tartrate, 68071-4598 — zolpidem tartrate, 68071-5063 — zolpidem tartrate, 68071-5093 — zolpidem tartrate, 68071-5120 — zolpidem tartrate, 68180-779 — Zolpidem Tartrate, 68788-7422 — Zolpidem Tartrate, 68788-8376 — Zolpidem Tartrate, 68788-8654 — Zolpidem Tartrate, 68788-8854 — Zolpidem Tartrate, 68788-9126 — zolpidem tartrate, 68788-9127 — zolpidem tartrate, 70518-2917 — zolpidem tartrate, 70518-3739 — Zolpidem Tartrate, 70518-3943 — Zolpidem Tartrate, 71093-155 — 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.