alrex

Generic: loteprednol etabonate

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

Drug Facts

Product Profile

Brand Name alrex
Generic Name loteprednol etabonate
Labeler bausch & lomb incorporated
Dosage Form SUSPENSION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

loteprednol etabonate 2 mg/mL

Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-353
Product ID 24208-353_138577af-1a4e-48fb-b088-47f54c896442
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020803
Listing Expiration 2026-12-31
Marketing Start 1998-03-09

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208353
Hyphenated Format 24208-353

Supplemental Identifiers

RxCUI
213262 311381
UPC
0324208353103
UNII
YEH1EZ96K6

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 alrex (source: ndc)
Generic Name loteprednol etabonate (source: ndc)
Application Number NDA020803 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (24208-353-01) / 1 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (24208-353-05) / 5 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (24208-353-10) / 10 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (3)

24208-353-01 1 BOTTLE, DROPPER in 1 CARTON (24208-353-01) / 1 mL in 1 BOTTLE, DROPPER 24208-353-05 1 BOTTLE, DROPPER in 1 CARTON (24208-353-05) / 5 mL in 1 BOTTLE, DROPPER 24208-353-10 1 BOTTLE, DROPPER in 1 CARTON (24208-353-10) / 10 mL in 1 BOTTLE, DROPPER

Ingredients (1)

loteprednol etabonate (2 mg/mL)

Linked Drug Pages (1)

Alrex ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "138577af-1a4e-48fb-b088-47f54c896442", "openfda": {"upc": ["0324208353103"], "unii": ["YEH1EZ96K6"], "rxcui": ["213262", "311381"], "spl_set_id": ["21c76da0-50a1-41c0-91b8-8cc4dcc27f60"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-353-01)  / 1 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-353-01", "marketing_start_date": "19980309"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-353-05)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-353-05", "marketing_start_date": "19980309"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-353-10)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-353-10", "marketing_start_date": "19980309"}], "brand_name": "Alrex", "product_id": "24208-353_138577af-1a4e-48fb-b088-47f54c896442", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "24208-353", "generic_name": "loteprednol etabonate", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alrex", "active_ingredients": [{"name": "LOTEPREDNOL ETABONATE", "strength": "2 mg/mL"}], "application_number": "NDA020803", "marketing_category": "NDA", "marketing_start_date": "19980309", "listing_expiration_date": "20261231"}