# promethazine hydrochloride

NDC: 27808-051
Generic name: promethazine hydrochloride
Labeler / Manufacturer: Cranbury Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SYRUP
Routes: ORAL
Marketing started: 20120608
Marketing ended: 20270301
FDA application: ANDA091675

## 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:"27808-051"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27808-051
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d32ea9db-11d4-400d-b7ef-dd0ec01b796d