Beryllium metallicum
- Product NDC
- 0220-0839
- 11-digit product format
- 002200839
- Labeler code
- 0220
- Product ID
- 0220-0839_09bab81a-261b-df3a-e063-6294a90a67dd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BERYLLIUM
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- BERYLLIUM
- Active strength
- 30 [hp_C]/30[hp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| OW5102UV6N | BERYLLIUM | 7440-41-7 | BERYLLIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-0839-41 | 00220083941 | 30 [hp_C] in 1 TUBE (0220-0839-41) | 1983-03-03 | No | No | Historical |