# Loperamide Hydrochloride

NDC: 63868-338
Generic name: Loperamide Hydrochloride
Labeler / Manufacturer: Chain Drug Marketing Association Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19930201

FDA application: ANDA074091

## Active ingredients

- LOPERAMIDE HYDROCHLORIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63868-338"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-338
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=237b845b-0f02-410d-9750-c95123e6142d