FDA.reportPublic FDA data

NDC 73687-062-80 - UPNEEQ

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
73687-062
Requested NDC
73687-062-80
Package NDCs from labels
73687-062-70, 73687-062-32, 73687-062-80, 73687-062-68, 73687-062-34, 73687-062-25, 73687-062-45
Manufacturer
RVL Pharmaceuticals, Inc.
Effective date
2026-07-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
UPNEEQ - RVL Pharmaceuticals, Inc.RVL Pharmaceuticals, Inc.2026-07-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73687-062-25UPNEEQ15 in 1 CARTONSOLUTION/ DROPS1529
73687-062-32UPNEEQ30 in 1 CARTONSOLUTION/ DROPS3029
73687-062-34UPNEEQ30 in 1 CARTONSOLUTION/ DROPS3029
73687-062-45UPNEEQ45 in 1 CARTONSOLUTION/ DROPS4529
73687-062-68UPNEEQ5 in 1 CARTONSOLUTION/ DROPS529
73687-062-70UPNEEQ.3 mL in 1 AMPULESOLUTION/ DROPS.329
73687-062-80UPNEEQ.3 mL in 1 AMPULESOLUTION/ DROPS.329

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73687-062UPNEEQ (OXYMETAZOLINE HYDROCHLORIDE OPHTHALMIC) SOLUTION/ DROPS [RVL PHARMACEUTICALS, INC.]28Current NDC, Legacy NDC, 7 package rows20241027_cf6c9a1f-2367-46d2-99c3-c7d67ec6f519.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
73687-062-32EA - Each73687-0627f823c2a-0818-4d4d-87ec-55b29cf1497912020-09-14
73687-062-45EA - Each73687-0624b5a94df-0df7-421d-830c-0c2751530f9b12022-01-06

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 83 of 83 · 1,644 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SODIUM CHLORIDESODIUM CHLORIDEBaxter Healthcare Corporationb3b4b176-41f0-4ca8-90d4-3fba5707564a2014-02-21Exact identifier
unii: 451W47IQ8X
TIS-U-SOLSODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATEBaxter Healthcare Corporation9da4121f-d62d-4da4-8dfb-0494da16015f2014-02-21Exact identifier
unii: 451W47IQ8X
unii: 660YQ98I10
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,Baxter Healthcare Corporatione1953d54-818d-46a6-8532-518ebae6d84e2012-06-13Exact identifier
unii: 451W47IQ8X
unii: 660YQ98I10
unii: M4I0D6VV5M
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEBaxter Healthcare Corporationf09f80bf-2f8b-4420-865d-aec2d5e5cd4d2012-06-12Exact identifier
unii: 451W47IQ8X
unii: 660YQ98I10
unii: M4I0D6VV5M

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.