NITROUS OXIDE
- Product NDC
- 10006-002
- 11-digit product format
- 100060002
- Labeler code
- 10006
- Product ID
- 10006-002_c4065ed6-237f-4545-bad2-a51e95a70949
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NITROUS OXIDE
- Dosage form
- GAS
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Acetylene Oxygen Company
- Marketing category
- UNAPPROVED MEDICAL GAS
- Marketing start
- 1936-01-01
- Marketing end
- 0000-00-00
- Substance
- NITROUS OXIDE
- Active strength
- 99 L/100L
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10006-002 | NITROUS OXIDE GAS [ACETYLENE OXYGEN COMPANY] | 1 | Legacy NDC | 20110428_689d269f-d3fc-4bea-8970-96697fc7cc92.zip |