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
- 71335-1693_30c2b613-bd3c-46d0-b344-cf46d7a9c616
- Product NDC
- 71335-1693
- Form
- TABLET
- Composition / generic term
- diphenoxylate hydrochloride and atropine sulfate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200315
- 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
- 20 TABLET in 1 BOTTLE (71335-1693-1) · 71335-1693-1
- 30 TABLET in 1 BOTTLE (71335-1693-2) · 71335-1693-2
- 15 TABLET in 1 BOTTLE (71335-1693-3) · 71335-1693-3
- 10 TABLET in 1 BOTTLE (71335-1693-4) · 71335-1693-4
- 40 TABLET in 1 BOTTLE (71335-1693-5) · 71335-1693-5
- 60 TABLET in 1 BOTTLE (71335-1693-6) · 71335-1693-6
- 90 TABLET in 1 BOTTLE (71335-1693-7) · 71335-1693-7
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 →