# PROMETHAZINE HYDROCHLORIDE

NDC: 81033-016
Generic name: PROMETHAZINE HYDROCHLORIDE
Labeler / Manufacturer: Kesin Pharma Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20241231

FDA application: ANDA040891

## Active ingredients

- PROMETHAZINE HYDROCHLORIDE: 6.25 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81033-016"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81033-016
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=28793bd2-bd40-4571-e063-6394a90ae789