NDC 49643-417 – American Elm Pollen

Ulmus Americana Pollen .05 g/mL · Injection · Cutaneous, Intradermal, Subcutaneous

Non-standardized Allergenic

Product NDC49643-417

Product details

Brand name
American Elm Pollen
Generic name
Ulmus americana
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 Pollen Allergenic Extract

Active ingredients

Package NDC codes (4)

Package NDCDescriptionSince
49643-417-055 mL in 1 VIAL, MULTI-DOSE (49643-417-05)Mar 12, 1974
49643-417-1010 mL in 1 VIAL, MULTI-DOSE (49643-417-10)Mar 12, 1974
49643-417-3030 mL in 1 VIAL, MULTI-DOSE (49643-417-30)Mar 12, 1974
49643-417-5050 mL in 1 VIAL, MULTI-DOSE (49643-417-50)Mar 12, 1974

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