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Nystatin
Nystatin - 21695-761-30 - (Nystatin)
Drug Information of Nystatin
| Product NDC: | 21695-761 |
| Proprietary Name: | Nystatin |
| Non Proprietary Name: | Nystatin |
| Active Ingredient(s): | 100000 mg/g & nbsp; Nystatin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nystatin
| Product NDC: | 21695-761 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064022 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930129 |
Package Information of Nystatin
| Package NDC: | 21695-761-30 |
| Package Description: | 1 TUBE in 1 CARTON (21695-761-30) > 30 g in 1 TUBE |
NDC Information of Nystatin
| NDC Code | 21695-761-30 |
| Proprietary Name | Nystatin |
| Package Description | 1 TUBE in 1 CARTON (21695-761-30) > 30 g in 1 TUBE |
| Product NDC | 21695-761 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nystatin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19930129 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | NYSTATIN |
| Strength Number | 100000 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |
