# Promethazine Hydrochloride

NDC: 51655-085
Generic name: Promethazine Hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140601

FDA application: ANDA091179

## Active ingredients

- PROMETHAZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-085"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-085
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ba4ec2d8-1da4-473b-9ef8-57051cb2c0f7