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American Cockroach - 49288-0150-1 - (American Cockroach)

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Drug Information of American Cockroach

Product NDC: 49288-0150
Proprietary Name: American Cockroach
Non Proprietary Name: American Cockroach
Active Ingredient(s): .02    g/mL & nbsp;   American Cockroach
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of American Cockroach

Product NDC: 49288-0150
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of American Cockroach

Package NDC: 49288-0150-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0150-1)

NDC Information of American Cockroach

NDC Code 49288-0150-1
Proprietary Name American Cockroach
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0150-1)
Product NDC 49288-0150
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name American Cockroach
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name PERIPLANETA AMERICANA
Strength Number .02
Strength Unit g/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 American Cockroach


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