| Product NDC: | 53489-400 |
| 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: | 53489-400 |
| Labeler Name: | Mutual Pharmaceutical Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062838 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19881222 |
| Package NDC: | 53489-400-02 |
| Package Description: | 50 TABLET, FILM COATED in 1 BOTTLE (53489-400-02) |
| NDC Code | 53489-400-02 |
| Proprietary Name | Nystatin |
| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (53489-400-02) |
| Product NDC | 53489-400 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nystatin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19881222 |
| Marketing Category Name | ANDA |
| Labeler Name | Mutual Pharmaceutical Company, Inc. |
| Substance Name | NYSTATIN |
| Strength Number | 500000 |
| Strength Unit | [USP'U]/1 |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |