# Promethazine Hydrochloride and Dextromethorphan Hydrobromide

NDC: 27808-057
Generic name: Promethazine Hydrochloride and Dextromethorphan Hydrobromide
Labeler / Manufacturer: Cranbury Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20140131
Marketing ended: 20270401
FDA application: ANDA091687

## Active ingredients

- DEXTROMETHORPHAN HYDROBROMIDE: 15 mg/5mL
- 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:"27808-057"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-057
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8b57027-a4b8-4149-93e8-aa3e7a6d6dc3