HELIUM
- Product NDC
- 10006-008
- 11-digit product format
- 100060008
- Labeler code
- 10006
- Product ID
- 10006-008_73d34d59-69b0-4bc0-b31d-617aa0d5b3fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HELIUM
- 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
- HELIUM
- 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 |
|---|
| 10006-008 | HELIUM GAS [ACETYLENE OXYGEN COMPANY] | 1 | Legacy NDC | 20110428_8c473d18-b656-4e00-8fbc-6e1128d41254.zip |