# Dicyclomine hydrochloride

NDC: 73352-119
Generic name: Dicyclomine hydrochloride
Labeler / Manufacturer: Trifluent Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250714

FDA application: ANDA216736

## Active ingredients

- DICYCLOMINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"73352-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73352-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56282794-5874-4220-b25c-cea4b17d19aa