Product NDC: | 54868-0243 |
Proprietary Name: | NYSTATIN |
Non Proprietary Name: | nystatin |
Active Ingredient(s): | 100000 [USP'U]/mL & nbsp; nystatin |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-0243 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062512 |
Marketing Category: | ANDA |
Start Marketing Date: | 19940328 |
Package NDC: | 54868-0243-0 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (54868-0243-0) > 473 mL in 1 BOTTLE, PLASTIC |
NDC Code | 54868-0243-0 |
Proprietary Name | NYSTATIN |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (54868-0243-0) > 473 mL in 1 BOTTLE, PLASTIC |
Product NDC | 54868-0243 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nystatin |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19940328 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | NYSTATIN |
Strength Number | 100000 |
Strength Unit | [USP'U]/mL |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |