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
- 72888-198_4b7e07c5-f687-74a5-e063-6294a90aa7ef
- Product NDC
- 72888-198
- Form
- TABLET
- Composition / generic term
- Dicyclomine hydrochloride
- Labeler
- Advagen Pharma Ltd.,
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250325
- Source listing expiry
- 20271231
Source-listed ingredients
- DICYCLOMINE HYDROCHLORIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (72888-198-00) · 72888-198-00
- 100 TABLET in 1 BOTTLE (72888-198-01) · 72888-198-01
- 500 TABLET in 1 BOTTLE (72888-198-05) · 72888-198-05
- 120 TABLET in 1 BOTTLE (72888-198-12) · 72888-198-12
- 30 TABLET in 1 BOTTLE (72888-198-30) · 72888-198-30
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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