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Nystatin
Nystatin - 66689-008-08 - (Nystatin)
Drug Information of Nystatin
| Product NDC: | 66689-008 |
| 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: | 66689-008 |
| Labeler Name: | VistaPharm Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065422 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120501 |
Package Information of Nystatin
| Package NDC: | 66689-008-08 |
| Package Description: | 237 mL in 1 BOTTLE (66689-008-08) |
NDC Information of Nystatin
| NDC Code | 66689-008-08 |
| Proprietary Name | Nystatin |
| Package Description | 237 mL in 1 BOTTLE (66689-008-08) |
| Product NDC | 66689-008 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nystatin |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20120501 |
| 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] |
