United States · FDA National Drug Code directory
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72189-336_2c3d9a97-2f79-1c66-e063-6294a90ab5c4
- Product NDC
- 72189-336
- Form
- TABLET
- Composition / generic term
- DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
- Labeler
- Direct Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220307
- Source listing expiry
- 20261231
Source-listed ingredients
- DIPHENOXYLATE HYDROCHLORIDE — 2.5 mg/1
- ATROPINE SULFATE — .025 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (72189-336-10) · 72189-336-10
- 30 TABLET in 1 BOTTLE (72189-336-30) · 72189-336-30
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →