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EQUUS CABALLUS SKIN - 0268-0628-30 - (HORSE EPITHELIA)

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Drug Information of EQUUS CABALLUS SKIN

Product NDC: 0268-0628
Proprietary Name: EQUUS CABALLUS SKIN
Non Proprietary Name: HORSE EPITHELIA
Active Ingredient(s): .1    g/mL & nbsp;   HORSE EPITHELIA
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of EQUUS CABALLUS SKIN

Product NDC: 0268-0628
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of EQUUS CABALLUS SKIN

Package NDC: 0268-0628-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (0268-0628-30)

NDC Information of EQUUS CABALLUS SKIN

NDC Code 0268-0628-30
Proprietary Name EQUUS CABALLUS SKIN
Package Description 30 mL in 1 VIAL, MULTI-DOSE (0268-0628-30)
Product NDC 0268-0628
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name HORSE EPITHELIA
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name EQUUS CABALLUS SKIN
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Animal Skin Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Cells, Epidermal [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of EQUUS CABALLUS SKIN


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