Mugwort - 36987-3269-1 - (Mugwort)

Alphabetical Index


Drug Information of Mugwort

Product NDC: 36987-3269
Proprietary Name: Mugwort
Non Proprietary Name: Mugwort
Active Ingredient(s): 10000    [PNU]/mL & nbsp;   Mugwort
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mugwort

Product NDC: 36987-3269
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Mugwort

Package NDC: 36987-3269-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-3269-1)

NDC Information of Mugwort

NDC Code 36987-3269-1
Proprietary Name Mugwort
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-3269-1)
Product NDC 36987-3269
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mugwort
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ARTEMISIA VULGARIS POLLEN
Strength Number 10000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Mugwort


General Information