NDC 49643-104 – Botrytis

Botrytis Cinerea .1 g/mL · Injection · Cutaneous, Intradermal, Subcutaneous

Non-standardized Allergenic

Product NDC49643-104

Product details

Brand name
Botrytis
Generic name
Botrytis cinerea
Labeler
Allermed Laboratories, Inc.
Dosage form
Injection
Route
Cutaneous, Intradermal, Subcutaneous
Marketing category
BLA · BLA102211
Marketed since
March 12, 1974
Listing expires
December 31, 2026
Pharmacologic class
Non-Standardized Fungal Allergenic Extract

Active ingredients

Package NDC codes (4)

Package NDCDescriptionSince
49643-104-055 mL in 1 VIAL, MULTI-DOSE (49643-104-05)Mar 12, 1974
49643-104-1010 mL in 1 VIAL, MULTI-DOSE (49643-104-10)Mar 12, 1974
49643-104-3030 mL in 1 VIAL, MULTI-DOSE (49643-104-30)Mar 12, 1974
49643-104-5050 mL in 1 VIAL, MULTI-DOSE (49643-104-50)Mar 12, 1974