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) |
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 NDC: | 66689-037-99 |
Package Description: | 10 TRAY in 1 CASE (66689-037-99) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-037-01) |
NDC Code | 66689-037-99 |
Proprietary Name | Nystatin |
Package Description | 10 TRAY in 1 CASE (66689-037-99) > 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] |