Home > National Drug Code (NDC) > Sheep Sorrel

Sheep Sorrel - 36987-3425-3 - (Sheep Sorrel)

Alphabetical Index


Drug Information of Sheep Sorrel

Product NDC: 36987-3425
Proprietary Name: Sheep Sorrel
Non Proprietary Name: Sheep Sorrel
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Sheep Sorrel
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sheep Sorrel

Product NDC: 36987-3425
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Sheep Sorrel

Package NDC: 36987-3425-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-3425-3)

NDC Information of Sheep Sorrel

NDC Code 36987-3425-3
Proprietary Name Sheep Sorrel
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-3425-3)
Product NDC 36987-3425
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sheep Sorrel
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name RUMEX ACETOSELLA POLLEN
Strength Number 40000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Increased Histamine Release [PE],Allergens [Chemical/Ingredient]

Complete Information of Sheep Sorrel


General Information