Kiwi - 36987-1417-4 - (Kiwi)

Alphabetical Index


Drug Information of Kiwi

Product NDC: 36987-1417
Proprietary Name: Kiwi
Non Proprietary Name: Kiwi
Active Ingredient(s): .1    g/mL & nbsp;   Kiwi
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kiwi

Product NDC: 36987-1417
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Kiwi

Package NDC: 36987-1417-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1417-4)

NDC Information of Kiwi

NDC Code 36987-1417-4
Proprietary Name Kiwi
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1417-4)
Product NDC 36987-1417
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Kiwi
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name KIWI FRUIT
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Kiwi


General Information