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Palmers Amaranth - 36987-3306-2 - (Palmers Amaranth)

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Drug Information of Palmers Amaranth

Product NDC: 36987-3306
Proprietary Name: Palmers Amaranth
Non Proprietary Name: Palmers Amaranth
Active Ingredient(s): .05    g/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: 36987-3306
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: 36987-3306-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-3306-2)

NDC Information of Palmers Amaranth

NDC Code 36987-3306-2
Proprietary Name Palmers Amaranth
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-3306-2)
Product NDC 36987-3306
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 .05
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 Palmers Amaranth


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