# Benzonatate

NDC: 68084-214
Generic name: Benzonatate
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210526

FDA application: ANDA040597

## 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:"68084-214"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-214
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9a71725a-64b6-4800-a79c-aa4b2d74d44f