Product NDC: | 59779-615 |
Proprietary Name: | antihistamine eye |
Non Proprietary Name: | Ketotifen |
Active Ingredient(s): | .25 mg/mL & nbsp; Ketotifen |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-615 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA077958 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101019 |
Package NDC: | 59779-615-01 |
Package Description: | 1 BOTTLE in 1 PACKAGE (59779-615-01) > 5 mL in 1 BOTTLE |
NDC Code | 59779-615-01 |
Proprietary Name | antihistamine eye |
Package Description | 1 BOTTLE in 1 PACKAGE (59779-615-01) > 5 mL in 1 BOTTLE |
Product NDC | 59779-615 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ketotifen |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20101019 |
Marketing Category Name | ANDA |
Labeler Name | CVS Pharmacy |
Substance Name | KETOTIFEN FUMARATE |
Strength Number | .25 |
Strength Unit | mg/mL |
Pharmaceutical Classes |