Product NDC: | 0023-4290 |
Proprietary Name: | LASTACAFT |
Non Proprietary Name: | alcaftadine |
Active Ingredient(s): | 2.5 mg/mL & nbsp; alcaftadine |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0023-4290 |
Labeler Name: | Allergan, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022134 |
Marketing Category: | NDA |
Start Marketing Date: | 20101101 |
Package NDC: | 0023-4290-03 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0023-4290-03) > 3 mL in 1 BOTTLE, PLASTIC |
NDC Code | 0023-4290-03 |
Proprietary Name | LASTACAFT |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0023-4290-03) > 3 mL in 1 BOTTLE, PLASTIC |
Product NDC | 0023-4290 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | alcaftadine |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20101101 |
Marketing Category Name | NDA |
Labeler Name | Allergan, Inc. |
Substance Name | ALCAFTADINE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |