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Cauliflower - 36987-1431-2 - (Cauliflower)

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Drug Information of Cauliflower

Product NDC: 36987-1431
Proprietary Name: Cauliflower
Non Proprietary Name: Cauliflower
Active Ingredient(s): .05    g/mL & nbsp;   Cauliflower
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cauliflower

Product NDC: 36987-1431
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Cauliflower

Package NDC: 36987-1431-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-1431-2)

NDC Information of Cauliflower

NDC Code 36987-1431-2
Proprietary Name Cauliflower
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-1431-2)
Product NDC 36987-1431
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cauliflower
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name CAULIFLOWER
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Vegetable Proteins [Chemical/Ingredient]

Complete Information of Cauliflower


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