Home NDC 50153-110 Oxygen
Product NDC 50153-110
11-digit product format 501530110
Labeler code 50153
Product ID 50153-110_49627f0f-f289-d45e-e063-6394a90aa4a9
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Oxygen
Dosage form GAS
Route RESPIRATORY (INHALATION)
Labeler Island Equipment Company
Marketing category UNAPPROVED MEDICAL GAS
Marketing start 1995-09-21
Substance OXYGEN
Active strength 99 L/100L
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 13 matching rows.
View current auxiliary records. · View the auxiliary file history.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Oxygen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXYGEN 99 L/100L
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination S88TT14065 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312172 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50153-110 OXYGEN GAS [ISLAND EQUIPMENT COMPANY] 115 Current NDC, Legacy NDC, 9 package rows 20241228_b2210399-35ec-4c29-a551-4b0e62a60408.zip
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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50153-110-07 50153011007 180 L in 1 DEWAR (50153-110-07) 180 l 1995-09-21 0000-00-00 No No Current 50153-110-10 50153011010 36 L in 1 DEWAR (50153-110-10) 36 l 1995-09-21 0000-00-00 No No Current 50153-110-11 50153011011 46 L in 1 DEWAR (50153-110-11) 46 l 1995-09-21 0000-00-00 No No Current 50153-110-12 50153011012 450 L in 1 DEWAR (50153-110-12) 450 l 1995-09-21 0000-00-00 No No Current 50153-110-13 50153011013 248 L in 1 CYLINDER (50153-110-13) 248 l 1995-09-21 0000-00-00 No No Current 50153-110-14 50153011014 415 L in 1 CYLINDER (50153-110-14) 415 l 1995-09-21 0000-00-00 No No Current 50153-110-15 50153011015 682 L in 1 CYLINDER (50153-110-15) 682 l 1995-09-21 0000-00-00 No No Current 50153-110-16 50153011016 3455 L in 1 CYLINDER (50153-110-16) 3455 l 1995-09-21 0000-00-00 No No Current 50153-110-17 50153011017 6910 L in 1 CYLINDER (50153-110-17) 6910 l 1995-09-21 0000-00-00 No No Current