Diphenoxylate Hydrochloride and Atropine Sulfate 2.5 mg / 0.025 mg tablet

Where it's made

This label doesn't name the factory that makes the drug (it lists 1 site that tests it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Mylan Pharmaceuticals Inc. names for other drugs.

Recalls

• Oct 20, 2017 · Class I · Pfizer Inc.
  SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent
  Lots: Lots: a) R83962, R93347, R93348, R93349, R93350, R93351, R93352, Exp. 2021 OCT 31; S57831, S57832, S57834, Exp. 2021 NOV 30 b) R93356, R93357, R93358, R97310, Exp. 2021 OCT 31.

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Atropine and Diphenoxylate: every company that makes it

Form

tablet, oral

Strength

2.5 mg / 0.025 mg

Approval

NDA authorized generic NDA012462

On the market since

Aug 7, 2012

Package NDCs

59762-1061-1 59762-1061-2

Official label

DailyMed (National Library of Medicine), updated Feb 23, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?