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Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 70518-3915 · REMEDYREPACK INC.

Generic namediphenoxylate hydrochloride and atropine sulfate
Dosage formTABLET
RouteORAL
Active ingredient(s)DIPHENOXYLATE HYDROCHLORIDE, ATROPINE SULFATE
Strength.025; 2.5 mg/1; mg/1
Pharmacologic classAnticholinergic [EPC], Antidiarrheal [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
DEA scheduleCV
Marketing categoryANDA

Packages

70518-3915-1 — 30 TABLET in 1 BLISTER PACK (70518-3915-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70069-481 — Atropine Sulfate monohydrate, 70069-581 — Atropine sulfate, 70069-582 — Atropine sulfate, 70069-583 — Atropine sulfate, 70069-631 — Atropine Sulfate, 70069-641 — Atropine Sulfate, 70069-716 — Atropine Sulfate Monohydrate, 70121-1705 — atropine sulfate, 70121-1706 — atropine sulfate, 70518-3120 — Atropine Sulfate, 70518-4188 — Atropine Sulfate, 70518-4329 — Atropine Sulfate, 70756-651 — Atropine Sulfate, 70756-652 — Atropine Sulfate, 70756-653 — Atropine Sulfate, 71205-909 — diphenoxylate hydrochloride and atropine sulfate, 71335-0311 — Diphenoxylate Hydrochloride and Atropine Sulfate, 71335-1693 — diphenoxylate hydrochloride and atropine sulfate, 71610-714 — diphenoxylate hydrochloride and atropine sulfate, 71610-809 — diphenoxylate hydrochloride and atropine sulfate, +96 more

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