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
- 70069-431_a927b130-5b1b-462f-bb0c-2ea8763487ee
- Product NDC
- 70069-431
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DICYCLOMINE HYDROCHLORIDE
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241105
- Source listing expiry
- 20261231
Source-listed ingredients
- DICYCLOMINE HYDROCHLORIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL in 1 CARTON (70069-431-05) / 2 mL in 1 VIAL (70069-431-01) · 70069-431-05
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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