United States · FDA National Drug Code directory
dicyclomine hydrochloride
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
- 0054-0885_14fe8389-11d7-49d9-94af-a6f164a77692
- Product NDC
- 0054-0885
- Form
- TABLET
- Composition / generic term
- dicyclomine hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260910
- Source listing expiry
- 20271231
Source-listed ingredients
- DICYCLOMINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (0054-0885-25) · 0054-0885-25
- 1000 TABLET in 1 BOTTLE, PLASTIC (0054-0885-31) · 0054-0885-31
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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