Aspen - 36987-2508-1 - (Aspen)

Alphabetical Index


Drug Information of Aspen

Product NDC: 36987-2508
Proprietary Name: Aspen
Non Proprietary Name: Aspen
Active Ingredient(s): .1    g/mL & nbsp;   Aspen
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aspen

Product NDC: 36987-2508
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Aspen

Package NDC: 36987-2508-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-2508-1)

NDC Information of Aspen

NDC Code 36987-2508-1
Proprietary Name Aspen
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-2508-1)
Product NDC 36987-2508
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Aspen
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name POPULUS TREMULOIDES POLLEN
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Aspen


General Information