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Zolpidem Tartrate

NDC 80425-0153 · Advanced Rx Pharmacy of Tennessee, 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 Receptor Positive Modulators [MoA], gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]
DEA scheduleCIV
Marketing categoryANDA

Packages

80425-0153-1 — 30 TABLET, FILM COATED in 1 BOTTLE (80425-0153-1)

80425-0153-2 — 60 TABLET, FILM COATED in 1 BOTTLE (80425-0153-2)

80425-0153-3 — 90 TABLET, FILM COATED in 1 BOTTLE (80425-0153-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72789-390 — Zolpidem Tartrate, 76420-233 — zolpidem tartrate, 76420-263 — zolpidem tartrate, 76420-318 — Zolpidem Tartrate, 76420-319 — Zolpidem Tartrate, 76420-416 — Zolpidem Tartrate, 76420-417 — Zolpidem Tartrate, 76420-494 — Zolpidem Tartrate, 76420-496 — Zolpidem Tartrate, 80425-0059 — Zolpidem Tartrate, 80425-0060 — Zolpidem Tartrate, 80425-0061 — Zolpidem Tartrate, 80425-0087 — Zolpidem Tartrate, 80425-0165 — Zolpidem Tartrate, 80425-0301 — Zolpidem Tartrate, 80425-0322 — Zolpidem Tartrate, 80425-0430 — Zolpidem Tartrate, 80425-0513 — Zolpidem Tartrate, 82868-064 — zolpidem tartrate, 82868-078 — 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.