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PYRETHRUM CINERARIIFOLIUM - 0268-0646-50 - (PYRETHRUM CINERARIIFOLIUM)

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Drug Information of PYRETHRUM CINERARIIFOLIUM

Product NDC: 0268-0646
Proprietary Name: PYRETHRUM CINERARIIFOLIUM
Non Proprietary Name: PYRETHRUM CINERARIIFOLIUM
Active Ingredient(s): .05    g/mL & nbsp;   PYRETHRUM CINERARIIFOLIUM
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PYRETHRUM CINERARIIFOLIUM

Product NDC: 0268-0646
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of PYRETHRUM CINERARIIFOLIUM

Package NDC: 0268-0646-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0646-50)

NDC Information of PYRETHRUM CINERARIIFOLIUM

NDC Code 0268-0646-50
Proprietary Name PYRETHRUM CINERARIIFOLIUM
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0646-50)
Product NDC 0268-0646
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name PYRETHRUM CINERARIIFOLIUM
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name PYRETHRUM CINERARIIFOLIUM
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient]

Complete Information of PYRETHRUM CINERARIIFOLIUM


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