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Benzonatate

NDC 23155-898 · HUMAN PRESCRIPTION DRUG · CAPSULE, LIQUID FILLED

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040682
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsBENZONATATE (100 mg/1)
Marketing started20240929
Package count2

External sources

Source: openFDA. Public-domain (CC0).