# TRIPROLIDINE HYDROCHLORIDE

NDC: 69367-450
Generic name: TRIPROLIDINE HYDROCHLORIDE
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN OTC DRUG
Marketing category: OTC monograph drug
Dosage form: SYRUP
Routes: ORAL
Marketing started: 20260810

FDA application: M012

## Active ingredients

- TRIPROLIDINE HYDROCHLORIDE: 1.25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-450"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-450
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4eeffb6d-fc5e-48bc-95f6-ec4d5cb6e0d2