GUNA-IL 2 - 17089-380-18 - (ALDESLEUKIN)

Alphabetical Index


Drug Information of GUNA-IL 2

Product NDC: 17089-380
Proprietary Name: GUNA-IL 2
Non Proprietary Name: ALDESLEUKIN
Active Ingredient(s): 4    [hp_C]/30mL & nbsp;   ALDESLEUKIN
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-IL 2

Product NDC: 17089-380
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20080617

Package Information of GUNA-IL 2

Package NDC: 17089-380-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-380-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-IL 2

NDC Code 17089-380-18
Proprietary Name GUNA-IL 2
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-380-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-380
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALDESLEUKIN
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20080617
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name ALDESLEUKIN
Strength Number 4
Strength Unit [hp_C]/30mL
Pharmaceutical Classes

Complete Information of GUNA-IL 2


General Information