# Dicyclomine Hydrochloride

NDC: 71335-2341
Generic name: Dicyclomine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230425

FDA application: ANDA040317

## Active ingredients

- DICYCLOMINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2341"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2341
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=226a3a6e-9419-448a-827f-01199b792762