Nystatin - 66689-037-50 - (Nystatin)

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Drug Information of Nystatin

Product NDC: 66689-037
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: 66689-037
Labeler Name: VistaPharm, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064142
Marketing Category: ANDA
Start Marketing Date: 20100510

Package Information of Nystatin

Package NDC: 66689-037-50
Package Description: 5 TRAY in 1 CASE (66689-037-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-037-01)

NDC Information of Nystatin

NDC Code 66689-037-50
Proprietary Name Nystatin
Package Description 5 TRAY in 1 CASE (66689-037-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-037-01)
Product NDC 66689-037
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nystatin
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20100510
Marketing Category Name ANDA
Labeler Name VistaPharm, Inc
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