# Galantamine

NDC: 70436-005
Generic name: galantamine
Labeler / Manufacturer: Slate Run Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170802

FDA application: ANDA077604

## Active ingredients

- GALANTAMINE HYDROBROMIDE: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70436-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70436-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56f365e5-0a23-4f69-e054-00144ff8d46c