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Pussy Willow - 49288-0609-4 - (Pussy Willow)

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Drug Information of Pussy Willow

Product NDC: 49288-0609
Proprietary Name: Pussy Willow
Non Proprietary Name: Pussy Willow
Active Ingredient(s): .05    g/mL & nbsp;   Pussy Willow
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Pussy Willow

Product NDC: 49288-0609
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19770909

Package Information of Pussy Willow

Package NDC: 49288-0609-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0609-4)

NDC Information of Pussy Willow

NDC Code 49288-0609-4
Proprietary Name Pussy Willow
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0609-4)
Product NDC 49288-0609
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pussy Willow
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19770909
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name SALIX DISCOLOR POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

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