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
- 63187-410_33e2fa6e-66b0-436e-8a4d-235f3ba2c94d
- Product NDC
- 63187-410
- Form
- TABLET
- Composition / generic term
- Dicyclomine Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990226
- Source listing expiry
- 20261231
Source-listed ingredients
- DICYCLOMINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (63187-410-15) · 63187-410-15
- 30 TABLET in 1 BOTTLE (63187-410-30) · 63187-410-30
- 60 TABLET in 1 BOTTLE (63187-410-60) · 63187-410-60
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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