# Loperamide Hydrochloride

NDC: 42799-605
Generic name: Loperamide Hydrochloride
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200925

FDA application: ANDA215001

## 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:"42799-605"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-605
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d92819f1-d02d-4959-a019-17d44df6ed2f