FDA NDC Directory · JSON-LD · Markdown

Winterfat Pollen

NDC 49643-348 · NON-STANDARDIZED ALLERGENIC · INJECTION

Generic nameEurotia lanata
Labeler / ManufacturerAllermed Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA102211
Dosage form / routeINJECTION · CUTANEOUS INTRADERMAL SUBCUTANEOUS
Active ingredientsKRASCHENINNIKOVIA LANATA POLLEN (.05 g/mL)
Marketing started19740312
Package count4

External sources

Source: openFDA. Public-domain (CC0).