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Nystop
Nystop - 0574-2008-15 - (Nystatin)
Drug Information of Nystop
| Product NDC: | 0574-2008 |
| Proprietary Name: | Nystop |
| 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) |
Labeler Information of Nystop
| Product NDC: | 0574-2008 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064118 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960816 |
Package Information of Nystop
| Package NDC: | 0574-2008-15 |
| Package Description: | 15 g in 1 BOTTLE, PLASTIC (0574-2008-15) |
NDC Information of Nystop
| NDC Code | 0574-2008-15 |
| Proprietary Name | Nystop |
| Package Description | 15 g in 1 BOTTLE, PLASTIC (0574-2008-15) |
| Product NDC | 0574-2008 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nystatin |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 19960816 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | NYSTATIN |
| Strength Number | 100000 |
| Strength Unit | [USP'U]/g |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |
