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Nystatin
Nystatin - 0093-0983-01 - (Nystatin)
Drug Information of Nystatin
| Product NDC: | 0093-0983 |
| 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) |
Labeler Information of Nystatin
| Product NDC: | 0093-0983 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062506 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Nystatin
| Package NDC: | 0093-0983-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0093-0983-01) |
NDC Information of Nystatin
| NDC Code | 0093-0983-01 |
| Proprietary Name | Nystatin |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0093-0983-01) |
| Product NDC | 0093-0983 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nystatin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | NYSTATIN |
| Strength Number | 500000 |
| Strength Unit | [USP'U]/1 |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |
