FDA NDC Directory · JSON-LD · Markdown

Lidocaine

NDC 51672-3020 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA086724
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsLIDOCAINE (50 mg/g)
Marketing started20130325
Package count2

External sources

Source: openFDA. Public-domain (CC0).