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Blackeye Pea - 36987-1620-3 - (Blackeye Pea)

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Drug Information of Blackeye Pea

Product NDC: 36987-1620
Proprietary Name: Blackeye Pea
Non Proprietary Name: Blackeye Pea
Active Ingredient(s): .1    g/mL & nbsp;   Blackeye Pea
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Blackeye Pea

Product NDC: 36987-1620
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Blackeye Pea

Package NDC: 36987-1620-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1620-3)

NDC Information of Blackeye Pea

NDC Code 36987-1620-3
Proprietary Name Blackeye Pea
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1620-3)
Product NDC 36987-1620
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Blackeye Pea
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name BLACK-EYED PEA
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient]

Complete Information of Blackeye Pea


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