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White Pepper - 36987-1722-4 - (White Pepper)

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Drug Information of White Pepper

Product NDC: 36987-1722
Proprietary Name: White Pepper
Non Proprietary Name: White Pepper
Active Ingredient(s): .05    g/mL & nbsp;   White Pepper
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of White Pepper

Product NDC: 36987-1722
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of White Pepper

Package NDC: 36987-1722-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1722-4)

NDC Information of White Pepper

NDC Code 36987-1722-4
Proprietary Name White Pepper
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1722-4)
Product NDC 36987-1722
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name White Pepper
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name WHITE PEPPER
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of White Pepper


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