Nystatin - 0121-4785-05 - (Nystatin)

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Drug Information of Nystatin

Product NDC: 0121-4785
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: 0121-4785
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062512
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Nystatin

Package NDC: 0121-4785-05
Package Description: 4 TRAY in 1 CASE (0121-4785-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE

NDC Information of Nystatin

NDC Code 0121-4785-05
Proprietary Name Nystatin
Package Description 4 TRAY in 1 CASE (0121-4785-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE
Product NDC 0121-4785
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nystatin
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, 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