Ancobon - 55154-6575-0 - (flucytosine)

Alphabetical Index


Drug Information of Ancobon

Product NDC: 55154-6575
Proprietary Name: Ancobon
Non Proprietary Name: flucytosine
Active Ingredient(s): 500    mg/1 & nbsp;   flucytosine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ancobon

Product NDC: 55154-6575
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017001
Marketing Category: NDA
Start Marketing Date: 19820101

Package Information of Ancobon

Package NDC: 55154-6575-0
Package Description: 10 POUCH in 1 BAG (55154-6575-0) > 1 CAPSULE in 1 POUCH

NDC Information of Ancobon

NDC Code 55154-6575-0
Proprietary Name Ancobon
Package Description 10 POUCH in 1 BAG (55154-6575-0) > 1 CAPSULE in 1 POUCH
Product NDC 55154-6575
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name flucytosine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19820101
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name FLUCYTOSINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antifungal [EPC]

Complete Information of Ancobon


General Information