# BENZTROPINE MESYLATE

NDC: 11534-167
Generic name: benztropine mesylate
Labeler / Manufacturer: SUNRISE PHARMACEUTICAL, INC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241016

FDA application: ANDA204713

## Active ingredients

- BENZTROPINE MESYLATE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11534-167"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11534-167
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2c988462-ce77-4e99-b98e-8f6ad519e295