Nystatin - 21695-761-15 - (Nystatin)

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Drug Information of Nystatin

Product NDC: 21695-761
Proprietary Name: Nystatin
Non Proprietary Name: Nystatin
Active Ingredient(s): 100000    mg/g & nbsp;   Nystatin
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Nystatin

Product NDC: 21695-761
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064022
Marketing Category: ANDA
Start Marketing Date: 19930129

Package Information of Nystatin

Package NDC: 21695-761-15
Package Description: 1 TUBE in 1 CARTON (21695-761-15) > 15 g in 1 TUBE

NDC Information of Nystatin

NDC Code 21695-761-15
Proprietary Name Nystatin
Package Description 1 TUBE in 1 CARTON (21695-761-15) > 15 g in 1 TUBE
Product NDC 21695-761
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nystatin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19930129
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name NYSTATIN
Strength Number 100000
Strength Unit mg/g
Pharmaceutical Classes Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient]

Complete Information of Nystatin


General Information