Watercress - 36987-1623-1 - (Watercress)

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Drug Information of Watercress

Product NDC: 36987-1623
Proprietary Name: Watercress
Non Proprietary Name: Watercress
Active Ingredient(s): .05    g/mL & nbsp;   Watercress
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Watercress

Product NDC: 36987-1623
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Watercress

Package NDC: 36987-1623-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-1623-1)

NDC Information of Watercress

NDC Code 36987-1623-1
Proprietary Name Watercress
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-1623-1)
Product NDC 36987-1623
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Watercress
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name WATERCRESS
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]

Complete Information of Watercress


General Information