Product NDC: | 68094-599 |
Proprietary Name: | Nystatin |
Non Proprietary Name: | Nystatin |
Active Ingredient(s): | 500000 [USP'U]/5mL & nbsp; Nystatin |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68094-599 |
Labeler Name: | Precision Dose, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062512 |
Marketing Category: | ANDA |
Start Marketing Date: | 20051215 |
Package NDC: | 68094-599-62 |
Package Description: | 3 TRAY in 1 CASE (68094-599-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-599-59) |
NDC Code | 68094-599-62 |
Proprietary Name | Nystatin |
Package Description | 3 TRAY in 1 CASE (68094-599-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-599-59) |
Product NDC | 68094-599 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nystatin |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20051215 |
Marketing Category Name | ANDA |
Labeler Name | Precision Dose, Inc. |
Substance Name | NYSTATIN |
Strength Number | 500000 |
Strength Unit | [USP'U]/5mL |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |