# Galantamine

NDC: 57237-050
Generic name: Galantamine
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110329

FDA application: ANDA090957

## Active ingredients

- GALANTAMINE HYDROBROMIDE: 8 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57237-050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57237-050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0dc1a93-b7b8-4179-8ea7-ceecbe1ef243