Product NDC: | 24208-402 |
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: | 24208-402 |
Labeler Name: | Bausch & Lomb Incorporated |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019907 |
Marketing Category: | NDA |
Start Marketing Date: | 19891229 |
Package NDC: | 24208-402-10 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-402-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Code | 24208-402-10 |
Proprietary Name | Metipranolol |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-402-10) > 10 mL in 1 BOTTLE, DROPPER |
Product NDC | 24208-402 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metipranolol |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 19891229 |
Marketing Category Name | NDA |
Labeler Name | Bausch & Lomb Incorporated |
Substance Name | METIPRANOLOL |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |