Product NDC: | 68308-152 |
Proprietary Name: | Nystatin |
Non Proprietary Name: | Nystatin |
Active Ingredient(s): | 100000 [USP'U]/g & nbsp; Nystatin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68308-152 |
Labeler Name: | Midlothian Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065203 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090915 |
Package NDC: | 68308-152-30 |
Package Description: | 30 g in 1 BOTTLE, PLASTIC (68308-152-30) |
NDC Code | 68308-152-30 |
Proprietary Name | Nystatin |
Package Description | 30 g in 1 BOTTLE, PLASTIC (68308-152-30) |
Product NDC | 68308-152 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nystatin |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20090915 |
Marketing Category Name | ANDA |
Labeler Name | Midlothian Laboratories, Inc. |
Substance Name | NYSTATIN |
Strength Number | 100000 |
Strength Unit | [USP'U]/g |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |