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Sunmark eye itch relief
Sunmark eye itch relief - 49348-163-17 - (Ketotifen Fumarate)
Drug Information of Sunmark eye itch relief
| Product NDC: | 49348-163 |
| Proprietary Name: | Sunmark 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) |
Labeler Information of Sunmark eye itch relief
| Product NDC: | 49348-163 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077958 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120221 |
Package Information of Sunmark eye itch relief
| Package NDC: | 49348-163-17 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-163-17) > 5 mL in 1 BOTTLE |
NDC Information of Sunmark eye itch relief
| NDC Code | 49348-163-17 |
| Proprietary Name | Sunmark eye itch relief |
| Package Description | 1 BOTTLE in 1 CARTON (49348-163-17) > 5 mL in 1 BOTTLE |
| Product NDC | 49348-163 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ketotifen Fumarate |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120221 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | KETOTIFEN FUMARATE |
| Strength Number | .25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
