Product NDC: | 62011-0105 |
Proprietary Name: | Health Mart eye itch relief |
Non Proprietary Name: | Ketotifen Fumarate |
Active Ingredient(s): | .25 mg/mL & nbsp; Ketotifen Fumarate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62011-0105 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA077958 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120203 |
Package NDC: | 62011-0105-1 |
Package Description: | 1 BOTTLE in 1 CARTON (62011-0105-1) > 5 mL in 1 BOTTLE |
NDC Code | 62011-0105-1 |
Proprietary Name | Health Mart eye itch relief |
Package Description | 1 BOTTLE in 1 CARTON (62011-0105-1) > 5 mL in 1 BOTTLE |
Product NDC | 62011-0105 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ketotifen Fumarate |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20120203 |
Marketing Category Name | ANDA |
Labeler Name | McKesson |
Substance Name | KETOTIFEN FUMARATE |
Strength Number | .25 |
Strength Unit | mg/mL |
Pharmaceutical Classes |