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Zaditor
Zaditor - 0065-4011-06 - (ketotifen fumarate)
Drug Information of Zaditor
| Product NDC: | 0065-4011 |
| Proprietary Name: | Zaditor |
| Non Proprietary Name: | ketotifen fumarate |
| Active Ingredient(s): | .35 mg/mL & nbsp; ketotifen fumarate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zaditor
| Product NDC: | 0065-4011 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077200 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121221 |
Package Information of Zaditor
| Package NDC: | 0065-4011-06 |
| Package Description: | 2 BOTTLE, DROPPER in 1 CARTON (0065-4011-06) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of Zaditor
| NDC Code | 0065-4011-06 |
| Proprietary Name | Zaditor |
| Package Description | 2 BOTTLE, DROPPER in 1 CARTON (0065-4011-06) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0065-4011 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ketotifen fumarate |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20121221 |
| Marketing Category Name | ANDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | KETOTIFEN FUMARATE |
| Strength Number | .35 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
