BOTRYTIS CINEREA
NDC 0268-8091 · ALK-Abello, Inc.
FDA carries 2 listing records for this NDC; the most recent is shown.
Generic nameBOTRYTIS CINEREA
Dosage formINJECTION, SOLUTION
RoutePERCUTANEOUS, SUBCUTANEOUS
Active ingredient(s)BOTRYTIS CINEREA
Strength.05 g/mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
Marketing categoryBLA
Packages
0268-8091-10 — 10.5 mL in 1 VIAL (0268-8091-10)
0268-8091-50 — 53 mL in 1 VIAL (0268-8091-50)
0268-8091-05 — 5.5 mL in 1 VIAL (0268-8091-05)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0268-8090 — BOTRYTIS CINEREA, 22840-1639 — Botrytis cinerea, 22840-2662 — Botrytis cinerea, 22840-5609 — Botrytis cinerea, 43406-0587 — Alternaria Alternata, Aspergillus Fumigatus, Botrytis Cinerea, Rhizopus Stolonifer, Ustilago Maydis, 49643-104 — Botrytis cinerea, 65044-5048 — Botrytis cinerea, 65044-5049 — Botrytis cinerea