Product NDC: | 61314-447 |
Proprietary Name: | Metipranolol |
Non Proprietary Name: | Metipranolol |
Active Ingredient(s): | 3 mg/mL & nbsp; Metipranolol |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-447 |
Labeler Name: | Falcon Pharmaceuticals, Ltd. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075720 |
Marketing Category: | ANDA |
Start Marketing Date: | 20010809 |
Package NDC: | 61314-447-10 |
Package Description: | 10 mL in 1 BOTTLE, PLASTIC (61314-447-10) |
NDC Code | 61314-447-10 |
Proprietary Name | Metipranolol |
Package Description | 10 mL in 1 BOTTLE, PLASTIC (61314-447-10) |
Product NDC | 61314-447 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metipranolol |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20010809 |
Marketing Category Name | ANDA |
Labeler Name | Falcon Pharmaceuticals, Ltd. |
Substance Name | METIPRANOLOL |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |