Helium
- Product NDC
- 21220-121
- 11-digit product format
- 212200121
- Labeler code
- 21220
- Product ID
- 21220-121_eb019e40-afe5-f003-e053-2995a90a409f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Helium
- Dosage form
- GAS
- Route
- RESPIRATORY (INHALATION)
- Labeler
- General Air Service & Supply Co
- Application
- NDA205912
- Marketing category
- NDA
- Marketing start
- 1958-01-01
- Marketing end
- 0000-00-00
- Substance
- HELIUM
- Active strength
- 990 mL/L
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21220-121-01 | 21220012101 | 6201 L in 1 CYLINDER (21220-121-01) | 6201 l | 1958-01-01 | 0000-00-00 | No | No | Current |
| 21220-121-02 | 21220012102 | 250 L in 1 CYLINDER (21220-121-02) | 250 l | 1958-01-01 | 0000-00-00 | No | No | Current |