FDA NDC Directory · JSON-LD · Markdown

Benzonatate

NDC 70518-4182 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA211518
Dosage form / routeCAPSULE · ORAL
Active ingredientsBENZONATATE (200 mg/1)
Marketing started20240924
Package count3

External sources

Source: openFDA. Public-domain (CC0).