Product NDC: | 0832-0465 |
Proprietary Name: | Nyamyc |
Non Proprietary Name: | Nystatin |
Active Ingredient(s): | 100000 [USP'U]/g & nbsp; Nystatin |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0832-0465 |
Labeler Name: | Upsher-Smith Laboratories Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065183 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050503 |
Package NDC: | 0832-0465-15 |
Package Description: | 15 g in 1 BOTTLE, PLASTIC (0832-0465-15) |
NDC Code | 0832-0465-15 |
Proprietary Name | Nyamyc |
Package Description | 15 g in 1 BOTTLE, PLASTIC (0832-0465-15) |
Product NDC | 0832-0465 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nystatin |
Dosage Form Name | POWDER |
Route Name | CUTANEOUS |
Start Marketing Date | 20050503 |
Marketing Category Name | ANDA |
Labeler Name | Upsher-Smith Laboratories Inc. |
Substance Name | NYSTATIN |
Strength Number | 100000 |
Strength Unit | [USP'U]/g |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |