| Product NDC: | 54868-5216 |
| Proprietary Name: | Nystatin |
| Non Proprietary Name: | nystatin |
| Active Ingredient(s): | 100000 [USP'U]/g & nbsp; nystatin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-5216 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064118 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050127 |
| Package NDC: | 54868-5216-0 |
| Package Description: | 15 g in 1 BOTTLE, PLASTIC (54868-5216-0) |
| NDC Code | 54868-5216-0 |
| Proprietary Name | Nystatin |
| Package Description | 15 g in 1 BOTTLE, PLASTIC (54868-5216-0) |
| Product NDC | 54868-5216 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nystatin |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20050127 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | NYSTATIN |
| Strength Number | 100000 |
| Strength Unit | [USP'U]/g |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |