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Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 43353-083 · Aphena Pharma Solutions - Tennessee, LLC

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 categoryNDA AUTHORIZED GENERIC

Packages

43353-083-30 — 30 TABLET in 1 BOTTLE (43353-083-30)

43353-083-53 — 60 TABLET in 1 BOTTLE (43353-083-53)

43353-083-60 — 90 TABLET in 1 BOTTLE (43353-083-60)

43353-083-70 — 120 TABLET in 1 BOTTLE (43353-083-70)

43353-083-80 — 180 TABLET in 1 BOTTLE (43353-083-80)

43353-083-90 — 240 TABLET in 1 BOTTLE (43353-083-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0641-6251 — Atropine Sulfate, 0641-6274 — Atropine Sulfate, 0641-6275 — Atropine Sulfate, 16729-483 — ATROPINE SULFATE, 16729-484 — ATROPINE SULFATE, 16729-512 — Atropine Sulfate, 17856-0125 — Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide, 24208-825 — Atropine Sulfate, 24208-965 — Atropine Sulfate, 42799-826 — Atropine sulfate, 43353-594 — Diphenoxylate Hydrochloride and Atropine Sulfate, 50090-3456 — Diphenoxylate Hydrochloride and Atropine Sulfate, 50090-5589 — diphenoxylate hydrochloride and atropine sulfate, 50090-5592 — diphenoxylate hydrochloride and atropine sulfate, 50090-5924 — Atropine Sulfate, 50090-7000 — Atropine Sulfate, 50090-7313 — atropine sulfate, 50742-665 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide, 50742-666 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide, 50742-667 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide, +96 more

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