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Carelessweed - 36987-3164-2 - (Carelessweed)

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Drug Information of Carelessweed

Product NDC: 36987-3164
Proprietary Name: Carelessweed
Non Proprietary Name: Carelessweed
Active Ingredient(s): .1    g/mL & nbsp;   Carelessweed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Carelessweed

Product NDC: 36987-3164
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Carelessweed

Package NDC: 36987-3164-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-3164-2)

NDC Information of Carelessweed

NDC Code 36987-3164-2
Proprietary Name Carelessweed
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-3164-2)
Product NDC 36987-3164
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carelessweed
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 .1
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 Carelessweed


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