Scandium Oxydatum
- Product NDC
- 37662-2989
- 11-digit product format
- 376622989
- Labeler code
- 37662
- Product ID
- 37662-2989_f9d0b7ba-bf4d-fe21-e053-6394a90a0621
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Scandium Oxydatum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Hahnemann Laboratories, INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-04-20
- Substance
- SCANDIUM OXIDE
- Active strength
- 6 [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| T0G94L07ZD | SCANDIUM OXIDE | 12060-08-1 | SCANDIUM OXIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 37662-2989-1 | 37662298901 | 200 PELLET in 1 VIAL, GLASS (37662-2989-1) | 200 pellet | 2023-04-20 | No | No | Historical |
| 37662-2989-2 | 37662298902 | 1200 PELLET in 1 BOTTLE, GLASS (37662-2989-2) | 1200 pellet | 2023-04-20 | No | No | Historical |
| 37662-2989-3 | 37662298903 | 4000 PELLET in 1 BOTTLE, GLASS (37662-2989-3) | 4000 pellet | 2023-04-20 | No | No | Historical |