Product NDC: | 0078-0476 |
Proprietary Name: | Zaditor |
Non Proprietary Name: | Ketotifen Fumarate |
Active Ingredient(s): | .345 mg/mL & nbsp; Ketotifen Fumarate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0078-0476 |
Labeler Name: | Novartis Pharmaceuticals Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021066 |
Marketing Category: | NDA |
Start Marketing Date: | 20090922 |
Package NDC: | 0078-0476-41 |
Package Description: | 2 BOTTLE, DROPPER in 1 CARTON (0078-0476-41) > 5 mL in 1 BOTTLE, DROPPER |
NDC Code | 0078-0476-41 |
Proprietary Name | Zaditor |
Package Description | 2 BOTTLE, DROPPER in 1 CARTON (0078-0476-41) > 5 mL in 1 BOTTLE, DROPPER |
Product NDC | 0078-0476 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ketotifen Fumarate |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20090922 |
Marketing Category Name | NDA |
Labeler Name | Novartis Pharmaceuticals Corporation |
Substance Name | KETOTIFEN FUMARATE |
Strength Number | .345 |
Strength Unit | mg/mL |
Pharmaceutical Classes |