# Loperamide Hydrochloride

NDC: 51660-123
Generic name: Loperamide Hydrochloride
Labeler / Manufacturer: Ohm Laboratories 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:"51660-123"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-123
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c26c15a1-3a8a-4562-8c5e-ebbc8b81e0c6