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Ketotifen Fumarate
Ketotifen Fumarate - 17478-717-10 - (Ketotifen Fumarate)
Drug Information of Ketotifen Fumarate
| Product NDC: | 17478-717 |
| Proprietary Name: | Ketotifen Fumarate |
| Non Proprietary Name: | Ketotifen Fumarate |
| Active Ingredient(s): | .35 mg/mL & nbsp; Ketotifen Fumarate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketotifen Fumarate
| Product NDC: | 17478-717 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077958 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071001 |
Package Information of Ketotifen Fumarate
| Package NDC: | 17478-717-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-717-10) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of Ketotifen Fumarate
| NDC Code | 17478-717-10 |
| Proprietary Name | Ketotifen Fumarate |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-717-10) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-717 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ketotifen Fumarate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20071001 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | KETOTIFEN FUMARATE |
| Strength Number | .35 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
