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
- 73473-902_98b3a053-2708-460d-9929-d89164cd4a49
- Product NDC
- 73473-902
- Form
- TABLET
- Composition / generic term
- DICYCLOMINE HYDROCHLORIDE
- Labeler
- Solaris Pharma Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250610
- Source listing expiry
- 20261231
Source-listed ingredients
- DICYCLOMINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (73473-902-01) · 73473-902-01
- 1000 TABLET in 1 BOTTLE (73473-902-10) · 73473-902-10
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 →