# Loperamide Hydrochloride

NDC: 46122-738
Generic name: Loperamide Hydrochloride
Labeler / Manufacturer: Amerisource Bergen
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230705

FDA application: ANDA206548

## 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:"46122-738"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-738
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c15f077-9f90-4262-9c17-a1ac70e45f57