APRICOT - 54575-336-02 - (apricot)

Alphabetical Index


Drug Information of APRICOT

Product NDC: 54575-336
Proprietary Name: APRICOT
Non Proprietary Name: apricot
Active Ingredient(s): 1    g/20mL & nbsp;   apricot
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of APRICOT

Product NDC: 54575-336
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of APRICOT

Package NDC: 54575-336-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-336-02)

NDC Information of APRICOT

NDC Code 54575-336-02
Proprietary Name APRICOT
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-336-02)
Product NDC 54575-336
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name apricot
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name APRICOT
Strength Number 1
Strength Unit g/20mL
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