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LEVOBUNOLOL HYDROCHLORIDE
LEVOBUNOLOL HYDROCHLORIDE - 60758-063-05 - (levobunolol hydrochloride)
Drug Information of LEVOBUNOLOL HYDROCHLORIDE
| Product NDC: | 60758-063 |
| Proprietary Name: | LEVOBUNOLOL HYDROCHLORIDE |
| Non Proprietary Name: | levobunolol hydrochloride |
| Active Ingredient(s): | 2.5 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: | 60758-063 |
| Labeler Name: | Pacific Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019814 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19970715 |
Package Information of LEVOBUNOLOL HYDROCHLORIDE
| Package NDC: | 60758-063-05 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (60758-063-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of LEVOBUNOLOL HYDROCHLORIDE
| NDC Code | 60758-063-05 |
| Proprietary Name | LEVOBUNOLOL HYDROCHLORIDE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (60758-063-05) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 60758-063 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levobunolol hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19970715 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Pacific Pharma, Inc. |
| Substance Name | LEVOBUNOLOL HYDROCHLORIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
