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OptiPranolol
OptiPranolol - 24208-275-07 - (metipranolol)
Drug Information of OptiPranolol
| Product NDC: | 24208-275 |
| Proprietary Name: | OptiPranolol |
| 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) |
Labeler Information of OptiPranolol
| Product NDC: | 24208-275 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019907 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19891229 |
Package Information of OptiPranolol
| Package NDC: | 24208-275-07 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-275-07) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of OptiPranolol
| NDC Code | 24208-275-07 |
| Proprietary Name | OptiPranolol |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-275-07) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-275 |
| 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] |
