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Palmers Amaranth - 36987-3304-3 - (Palmers Amaranth)

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Drug Information of Palmers Amaranth

Product NDC: 36987-3304
Proprietary Name: Palmers Amaranth
Non Proprietary Name: Palmers Amaranth
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Palmers Amaranth
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Palmers Amaranth

Product NDC: 36987-3304
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Palmers Amaranth

Package NDC: 36987-3304-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-3304-3)

NDC Information of Palmers Amaranth

NDC Code 36987-3304-3
Proprietary Name Palmers Amaranth
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-3304-3)
Product NDC 36987-3304
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Palmers Amaranth
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name AMARANTHUS PALMERI POLLEN
Strength Number 20000
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]

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