| Product NDC: | 55154-8252 |
| Proprietary Name: | Nystatin |
| Non Proprietary Name: | Nystatin |
| Active Ingredient(s): | 500000 [USP'U]/1 & nbsp; Nystatin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-8252 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062506 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19840116 |
| Package NDC: | 55154-8252-0 |
| Package Description: | 10 POUCH in 1 BAG (55154-8252-0) > 1 TABLET, FILM COATED in 1 POUCH |
| NDC Code | 55154-8252-0 |
| Proprietary Name | Nystatin |
| Package Description | 10 POUCH in 1 BAG (55154-8252-0) > 1 TABLET, FILM COATED in 1 POUCH |
| Product NDC | 55154-8252 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nystatin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19840116 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | NYSTATIN |
| Strength Number | 500000 |
| Strength Unit | [USP'U]/1 |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |