Nystatin - 68308-152-30 - (Nystatin)

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Drug Information of Nystatin

Product NDC: 68308-152
Proprietary Name: Nystatin
Non Proprietary Name: Nystatin
Active Ingredient(s): 100000    [USP'U]/g & nbsp;   Nystatin
Administration Route(s): TOPICAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of Nystatin

Product NDC: 68308-152
Labeler Name: Midlothian Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065203
Marketing Category: ANDA
Start Marketing Date: 20090915

Package Information of Nystatin

Package NDC: 68308-152-30
Package Description: 30 g in 1 BOTTLE, PLASTIC (68308-152-30)

NDC Information of Nystatin

NDC Code 68308-152-30
Proprietary Name Nystatin
Package Description 30 g in 1 BOTTLE, PLASTIC (68308-152-30)
Product NDC 68308-152
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nystatin
Dosage Form Name POWDER
Route Name TOPICAL
Start Marketing Date 20090915
Marketing Category Name ANDA
Labeler Name Midlothian Laboratories, Inc.
Substance Name NYSTATIN
Strength Number 100000
Strength Unit [USP'U]/g
Pharmaceutical Classes Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient]

Complete Information of Nystatin


General Information