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
- 71335-0311_758bb992-fe97-4c59-aad1-7b3f7401fd47
- Product NDC
- 71335-0311
- Form
- TABLET
- Composition / generic term
- Diphenoxylate Hydrochloride and Atropine Sulfate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170707
- Source listing expiry
- 20271231
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 (71335-0311-1) · 71335-0311-1
- 30 TABLET in 1 BOTTLE (71335-0311-2) · 71335-0311-2
- 15 TABLET in 1 BOTTLE (71335-0311-3) · 71335-0311-3
- 10 TABLET in 1 BOTTLE (71335-0311-4) · 71335-0311-4
- 40 TABLET in 1 BOTTLE (71335-0311-5) · 71335-0311-5
- 60 TABLET in 1 BOTTLE (71335-0311-6) · 71335-0311-6
- 90 TABLET in 1 BOTTLE (71335-0311-7) · 71335-0311-7
Source and coverage
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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.
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