# Loperamide Hydrochloride

NDC: 43598-770
Generic name: Loperamide Hydrochloride
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20211022

FDA application: ANDA213070

## 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:"43598-770"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-770
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fe91ddc-06b6-3a51-2b48-f6f11361ab73