Oxygen
- Product NDC
- 57999-001
- Requested package NDC
- 57999-001-08
- 11-digit product format
- 579990001
- Labeler code
- 57999
- Product ID
- 57999-001_d359f7d9-d7f5-8d51-e053-2a95a90a26a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxygen
- Dosage form
- GAS
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Bay View Homecare, Inc.
- Marketing category
- UNAPPROVED MEDICAL GAS
- Marketing start
- 2003-05-01
- Marketing end
- 0000-00-00
- Substance
- OXYGEN
- Active strength
- 99 L/100L
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57999-001 | OXYGEN GAS [BAY VIEW HOMECARE, INC] | 100 | Legacy NDC, 10 package rows | 20240127_81f650d2-f6b9-6289-e053-2a91aa0a86e3.zip |
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 |
|---|
| 57999-001-08 | 57999000108 | 21 L in 1 DEWAR (57999-001-08) | 21 l | 2011-05-05 | 0000-00-00 | No | No | Current |