Nystatin - 54569-1018-0 - (Nystatin)

Alphabetical Index


Drug Information of Nystatin

Product NDC: 54569-1018
Proprietary Name: Nystatin
Non Proprietary Name: Nystatin
Active Ingredient(s): 100000    [USP'U]/mL & nbsp;   Nystatin
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Nystatin

Product NDC: 54569-1018
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062876
Marketing Category: ANDA
Start Marketing Date: 19880229

Package Information of Nystatin

Package NDC: 54569-1018-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (54569-1018-0) > 60 mL in 1 BOTTLE, DROPPER

NDC Information of Nystatin

NDC Code 54569-1018-0
Proprietary Name Nystatin
Package Description 1 BOTTLE, DROPPER in 1 CARTON (54569-1018-0) > 60 mL in 1 BOTTLE, DROPPER
Product NDC 54569-1018
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nystatin
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 19880229
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name NYSTATIN
Strength Number 100000
Strength Unit [USP'U]/mL
Pharmaceutical Classes Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient]

Complete Information of Nystatin


General Information