FDA NDC Directory · JSON-LD · Markdown

Standardized Redtop Grass

NDC 49643-309 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameAgrostis alba
Labeler / ManufacturerAllermed Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA102218
Dosage form / routeINJECTION · CUTANEOUS INTRADERMAL SUBCUTANEOUS
Active ingredientsAGROSTIS GIGANTEA POLLEN (100000 [BAU]/mL)
Marketing started19961202
Package count4

External sources

Source: openFDA. Public-domain (CC0).