Product NDC: | 0168-0007 |
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) |
Product NDC: | 0168-0007 |
Labeler Name: | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062124 |
Marketing Category: | ANDA |
Start Marketing Date: | 19820923 |
Package NDC: | 0168-0007-15 |
Package Description: | 15 g in 1 TUBE (0168-0007-15) |
NDC Code | 0168-0007-15 |
Proprietary Name | Nystatin |
Package Description | 15 g in 1 TUBE (0168-0007-15) |
Product NDC | 0168-0007 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nystatin |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19820923 |
Marketing Category Name | ANDA |
Labeler Name | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
Substance Name | NYSTATIN |
Strength Number | 100000 |
Strength Unit | [USP'U]/g |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |