Poppyseed - 36987-1731-4 - (Poppyseed)

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Drug Information of Poppyseed

Product NDC: 36987-1731
Proprietary Name: Poppyseed
Non Proprietary Name: Poppyseed
Active Ingredient(s): .05    g/mL & nbsp;   Poppyseed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Poppyseed

Product NDC: 36987-1731
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Poppyseed

Package NDC: 36987-1731-4
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-1731-4)

NDC Information of Poppyseed

NDC Code 36987-1731-4
Proprietary Name Poppyseed
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-1731-4)
Product NDC 36987-1731
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Poppyseed
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name POPPY SEED
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Seed Storage Proteins [Chemical/Ingredient]

Complete Information of Poppyseed


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