Home > National Drug Code (NDC) > Fremont Cottonwood Pollen

Fremont Cottonwood Pollen - 49643-396-30 - (Populus fremontii)

Alphabetical Index


Drug Information of Fremont Cottonwood Pollen

Product NDC: 49643-396
Proprietary Name: Fremont Cottonwood Pollen
Non Proprietary Name: Populus fremontii
Active Ingredient(s): 1    g/20mL & nbsp;   Populus fremontii
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fremont Cottonwood Pollen

Product NDC: 49643-396
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Fremont Cottonwood Pollen

Package NDC: 49643-396-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49643-396-30)

NDC Information of Fremont Cottonwood Pollen

NDC Code 49643-396-30
Proprietary Name Fremont Cottonwood Pollen
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49643-396-30)
Product NDC 49643-396
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Populus fremontii
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name POPULUS FREMONTII POLLEN
Strength Number 1
Strength Unit g/20mL
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]

Complete Information of Fremont Cottonwood Pollen


General Information