# Galantamine Hydrobromide

NDC: 47335-837
Generic name: Galantamine Hydrobromide
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20110209

FDA application: ANDA090178

## Active ingredients

- GALANTAMINE HYDROBROMIDE: 24 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-837"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-837
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1697161-ebe8-42b0-83e7-c9de4412546c