# Dicyclomine Hydrochloride

NDC: 0527-1282
Generic name: Dicyclomine Hydrochloride
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19990226

FDA application: ANDA040230

## Active ingredients

- DICYCLOMINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-1282"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-1282
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bd2cba10-70ec-4d1f-b46c-53d1de2ee130