FDA NDC Directory · JSON-LD · Markdown

Vanilla

NDC 22840-5754 · NON-STANDARDIZED ALLERGENIC · SOLUTION

Generic nameVanilla planifolia
Labeler / ManufacturerGreer Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA101833
Dosage form / routeSOLUTION · INTRADERMAL PERCUTANEOUS SUBCUTANEOUS
Active ingredientsVANILLA (.05 g/mL)
Marketing started19810915
Package count2

External sources

Source: openFDA. Public-domain (CC0).