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Nystatin
Nystatin - 0472-0166-15 - (Nystatin)
Drug Information of Nystatin
| Product NDC: | 0472-0166 |
| Proprietary Name: | Nystatin |
| Non Proprietary Name: | Nystatin |
| Active Ingredient(s): | 100000 [USP'U]/g & nbsp; Nystatin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nystatin
| Product NDC: | 0472-0166 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062840 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020903 |
Package Information of Nystatin
| Package NDC: | 0472-0166-15 |
| Package Description: | 1 TUBE in 1 CARTON (0472-0166-15) > 15 g in 1 TUBE |
NDC Information of Nystatin
| NDC Code | 0472-0166-15 |
| Proprietary Name | Nystatin |
| Package Description | 1 TUBE in 1 CARTON (0472-0166-15) > 15 g in 1 TUBE |
| Product NDC | 0472-0166 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nystatin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20020903 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | NYSTATIN |
| Strength Number | 100000 |
| Strength Unit | [USP'U]/g |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |
