levobunolol hydrochloride

Generic: levobunolol hydrochloride

Labeler: bausch & lomb incorporated
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levobunolol hydrochloride
Generic Name levobunolol hydrochloride
Labeler bausch & lomb incorporated
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

levobunolol hydrochloride 5 mg/mL

Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-505
Product ID 24208-505_1e033456-2f30-9208-e063-6394a90a094f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074326
Listing Expiration 2026-12-31
Marketing Start 1994-03-04

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208505
Hyphenated Format 24208-505

Supplemental Identifiers

RxCUI
1150836
UNII
O90S49LDHH

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name levobunolol hydrochloride (source: ndc)
Generic Name levobunolol hydrochloride (source: ndc)
Application Number ANDA074326 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (24208-505-05) / 5 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (24208-505-10) / 10 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (24208-505-15) / 15 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (3)

24208-505-05 1 BOTTLE, DROPPER in 1 CARTON (24208-505-05) / 5 mL in 1 BOTTLE, DROPPER 24208-505-10 1 BOTTLE, DROPPER in 1 CARTON (24208-505-10) / 10 mL in 1 BOTTLE, DROPPER 24208-505-15 1 BOTTLE, DROPPER in 1 CARTON (24208-505-15) / 15 mL in 1 BOTTLE, DROPPER

Ingredients (1)

levobunolol hydrochloride (5 mg/mL)

Linked Drug Pages (1)

Levobunolol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "1e033456-2f30-9208-e063-6394a90a094f", "openfda": {"unii": ["O90S49LDHH"], "rxcui": ["1150836"], "spl_set_id": ["5ab1efbe-530b-4787-b40a-c7dbf18161e1"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-505-05)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-505-05", "marketing_start_date": "19940304"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-505-10)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-505-10", "marketing_start_date": "19940304"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-505-15)  / 15 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-505-15", "marketing_start_date": "19940304"}], "brand_name": "Levobunolol Hydrochloride", "product_id": "24208-505_1e033456-2f30-9208-e063-6394a90a094f", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "24208-505", "generic_name": "Levobunolol Hydrochloride", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levobunolol Hydrochloride", "active_ingredients": [{"name": "LEVOBUNOLOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA074326", "marketing_category": "ANDA", "marketing_start_date": "19940304", "listing_expiration_date": "20261231"}