| NDC Code | 24208-505-10 |
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| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-505-10) / 10 mL in 1 BOTTLE, DROPPER |
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| Product NDC | 24208-505 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Levobunolol Hydrochloride |
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| Non-Proprietary Name | Levobunolol Hydrochloride |
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| Dosage Form | SOLUTION/ DROPS |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 19940304 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074326 |
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| Manufacturer | Bausch & Lomb Incorporated |
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| Substance Name | LEVOBUNOLOL HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
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