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Loperamide Hydrochloride

NDC 58602-701 · Aurohealth LLC

Generic nameLoperamide Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)LOPERAMIDE HYDROCHLORIDE
Strength2 mg/1
Pharmacologic classOpioid Agonist [EPC], Opioid Agonists [MoA]
Marketing categoryANDA

Packages

58602-701-01 — 1 BLISTER PACK in 1 CARTON (58602-701-01) / 6 TABLET in 1 BLISTER PACK

58602-701-02 — 2 BLISTER PACK in 1 CARTON (58602-701-02) / 6 TABLET in 1 BLISTER PACK

58602-701-76 — 4 BLISTER PACK in 1 CARTON (58602-701-76) / 6 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55319-375 — Loperamide HCl, 55910-155 — Loperamide Hydrochloride, 55910-176 — LOPERAMIDE HYDROCHLORIDE, 55910-224 — Loperamide Hydrochloride, 55910-375 — Loperamide HCl, 55910-383 — loperamide hydrochloride, simethicone, 55910-867 — loperamide HCl, 56062-224 — Loperamide Hydrochloride, 56062-680 — LOPERAMIDE HYDROCHLORIDE, 57896-381 — Loperamide HCl, 58602-727 — LOPERAMIDE HYDROCHLORIDE, 58602-815 — Loperamide Hydrochloride and Simethicone, 58602-868 — Loperamide Hydrochloride and Simethicone, 58602-869 — Loperamide Hydrochloride and Simethicone, 58602-870 — Loperamide Hydrochloride, 59556-959 — Loperamide Hydrochloride, 59651-691 — LOPERAMIDE HYDROCHLORIDE, 59779-700 — Loperamide Hydrochloride, 59779-960 — Loperamide HCl, 60468-005 — LOPERAMIDE HYDROCHLORIDE, +215 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.