Apricot - 49288-0011-2 - (Apricot)

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Drug Information of Apricot

Product NDC: 49288-0011
Proprietary Name: Apricot
Non Proprietary Name: Apricot
Active Ingredient(s): 1    mL/mL & nbsp;   Apricot
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Apricot

Product NDC: 49288-0011
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Apricot

Package NDC: 49288-0011-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0011-2)

NDC Information of Apricot

NDC Code 49288-0011-2
Proprietary Name Apricot
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0011-2)
Product NDC 49288-0011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Apricot
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name APRICOT
Strength Number 1
Strength Unit mL/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Fruit Proteins [Chemical/Ingredient]

Complete Information of Apricot


General Information