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Cockroach American - 36987-1796-2 - (Cockroach American)

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Drug Information of Cockroach American

Product NDC: 36987-1796
Proprietary Name: Cockroach American
Non Proprietary Name: Cockroach American
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Cockroach American
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cockroach American

Product NDC: 36987-1796
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Cockroach American

Package NDC: 36987-1796-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-1796-2)

NDC Information of Cockroach American

NDC Code 36987-1796-2
Proprietary Name Cockroach American
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-1796-2)
Product NDC 36987-1796
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cockroach American
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ALLERGENIC EXTRACT- COCKROACH PERIPLANETA AMERICANA
Strength Number 20000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Insect Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Insect Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Cockroach American


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