# Loperamide hydrochloride

NDC: 70771-1769
Generic name: Loperamide hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230625

FDA application: ANDA217471

## 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:"70771-1769"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1769
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5d13405c-8fd7-454f-9b49-3d8b9ef672b8