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Cat Pelt, Standardized - 0268-0269-05 - (Cat Pelt, Standardized)

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Drug Information of Cat Pelt, Standardized

Product NDC: 0268-0269
Proprietary Name: Cat Pelt, Standardized
Non Proprietary Name: Cat Pelt, Standardized
Active Ingredient(s): 100    [BAU]/mL & nbsp;   Cat Pelt, Standardized
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cat Pelt, Standardized

Product NDC: 0268-0269
Labeler Name: ALK-Abello, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103061
Marketing Category: BLA
Start Marketing Date: 19920924

Package Information of Cat Pelt, Standardized

Package NDC: 0268-0269-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-0269-05)

NDC Information of Cat Pelt, Standardized

NDC Code 0268-0269-05
Proprietary Name Cat Pelt, Standardized
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-0269-05)
Product NDC 0268-0269
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cat Pelt, Standardized
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19920924
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name FELIS CATUS SKIN
Strength Number 100
Strength Unit [BAU]/mL
Pharmaceutical Classes Standardized Animal Pelt Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fur [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Cat Pelt, Standardized


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