Product NDC: | 0472-0166 |
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: | 0472-0166 |
Labeler Name: | Actavis Mid Atlantic LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062840 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020903 |
Package NDC: | 0472-0166-30 |
Package Description: | 1 TUBE in 1 CARTON (0472-0166-30) > 30 g in 1 TUBE |
NDC Code | 0472-0166-30 |
Proprietary Name | Nystatin |
Package Description | 1 TUBE in 1 CARTON (0472-0166-30) > 30 g in 1 TUBE |
Product NDC | 0472-0166 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nystatin |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20020903 |
Marketing Category Name | ANDA |
Labeler Name | Actavis Mid Atlantic LLC |
Substance Name | NYSTATIN |
Strength Number | 100000 |
Strength Unit | [USP'U]/g |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |