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Rough (Redroot) Pigweed - 49288-0408-3 - (Rough (Redroot) Pigweed)

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Drug Information of Rough (Redroot) Pigweed

Product NDC: 49288-0408
Proprietary Name: Rough (Redroot) Pigweed
Non Proprietary Name: Rough (Redroot) Pigweed
Active Ingredient(s): .1    g/mL & nbsp;   Rough (Redroot) Pigweed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rough (Redroot) Pigweed

Product NDC: 49288-0408
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Rough (Redroot) Pigweed

Package NDC: 49288-0408-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0408-3)

NDC Information of Rough (Redroot) Pigweed

NDC Code 49288-0408-3
Proprietary Name Rough (Redroot) Pigweed
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0408-3)
Product NDC 49288-0408
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rough (Redroot) Pigweed
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name AMARANTHUS RETROFLEXUS POLLEN
Strength Number .1
Strength Unit g/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 Rough (Redroot) Pigweed


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