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Levobunolol Hydrochloride
Levobunolol Hydrochloride - 24208-505-15 - (Levobunolol Hydrochloride)
Drug Information of Levobunolol Hydrochloride
| Product NDC: | 24208-505 |
| Proprietary Name: | Levobunolol Hydrochloride |
| Non Proprietary Name: | Levobunolol Hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; Levobunolol Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levobunolol Hydrochloride
| Product NDC: | 24208-505 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074326 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19940304 |
Package Information of Levobunolol Hydrochloride
| Package NDC: | 24208-505-15 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-505-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of Levobunolol Hydrochloride
| NDC Code | 24208-505-15 |
| Proprietary Name | Levobunolol Hydrochloride |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-505-15) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-505 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levobunolol Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19940304 |
| Marketing Category Name | ANDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | LEVOBUNOLOL HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
