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Black Willow - 36987-3089-2 - (Black Willow)

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Drug Information of Black Willow

Product NDC: 36987-3089
Proprietary Name: Black Willow
Non Proprietary Name: Black Willow
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Black Willow
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Black Willow

Product NDC: 36987-3089
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Black Willow

Package NDC: 36987-3089-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-3089-2)

NDC Information of Black Willow

NDC Code 36987-3089-2
Proprietary Name Black Willow
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-3089-2)
Product NDC 36987-3089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Black Willow
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name SALIX NIGRA POLLEN
Strength Number 40000
Strength Unit [PNU]/mL
Pharmaceutical Classes

Complete Information of Black Willow


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