United States · FDA National Drug Code directory
Lomotil
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
- 0025-0061_69fba82d-8e83-4efb-8c88-5175fda71617
- Product NDC
- 0025-0061
- Form
- TABLET
- Composition / generic term
- diphenoxylate hydrochloride and atropine sulfate
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Marketing category
- NDA
- Marketing start / end (source format)
- 19600915
- 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
- 100 TABLET in 1 BOTTLE (0025-0061-31) · 0025-0061-31
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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