# Benzonatate

NDC: 68788-7607
Generic name: Benzonatate
Labeler / Manufacturer: Preferred Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200207

FDA application: ANDA206948

## Active ingredients

- BENZONATATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-7607"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7607
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3309040d-e240-42f6-9c51-5c54604a3896