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False Ragweed - 36987-3367-4 - (False Ragweed)

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Drug Information of False Ragweed

Product NDC: 36987-3367
Proprietary Name: False Ragweed
Non Proprietary Name: False Ragweed
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   False Ragweed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of False Ragweed

Product NDC: 36987-3367
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of False Ragweed

Package NDC: 36987-3367-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-3367-4)

NDC Information of False Ragweed

NDC Code 36987-3367-4
Proprietary Name False Ragweed
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-3367-4)
Product NDC 36987-3367
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name False Ragweed
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name AMBROSIA ACANTHICARPA POLLEN
Strength Number 20000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of False Ragweed


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