Product NDC: | 53489-400 |
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) |
Product NDC: | 53489-400 |
Labeler Name: | Mutual Pharmaceutical Company, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062838 |
Marketing Category: | ANDA |
Start Marketing Date: | 19881222 |
Package NDC: | 53489-400-10 |
Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (53489-400-10) |
NDC Code | 53489-400-10 |
Proprietary Name | Nystatin |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (53489-400-10) |
Product NDC | 53489-400 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nystatin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19881222 |
Marketing Category Name | ANDA |
Labeler Name | Mutual Pharmaceutical Company, Inc. |
Substance Name | NYSTATIN |
Strength Number | 500000 |
Strength Unit | [USP'U]/1 |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |