# PROMETHEGAN

NDC: 0713-0132
Generic name: promethazine hydrochloride
Labeler / Manufacturer: Cosette Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUPPOSITORY
Routes: RECTAL
Marketing started: 19870831

FDA application: ANDA087165

## Active ingredients

- PROMETHAZINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0713-0132"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0713-0132
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=636bb9bc-0cc5-4d6a-85be-6471acf01ffc