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
- 24979-200_d1cace55-0a40-4a47-a4d9-d57ed5035686
- Product NDC
- 24979-200
- Form
- TABLET
- Composition / generic term
- Dicyclomine Hydrochloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230701
- 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 (24979-200-01) · 24979-200-01
- 500 TABLET in 1 BOTTLE, PLASTIC (24979-200-02) · 24979-200-02
- 1000 TABLET in 1 BOTTLE, PLASTIC (24979-200-03) · 24979-200-03
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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