# Loperamide HCl

NDC: 50844-735
Generic name: Loperamide HCl
Labeler / Manufacturer: L.N.K. International, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20050503

FDA application: ANDA076497

## 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:"50844-735"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50844-735
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=547c4197-f573-4b30-9e39-2ab11d343609