MEDULLA OSSIS SUIS
- Product NDC
- 0220-3329
- 11-digit product format
- 002203329
- Labeler code
- 0220
- Product ID
- 0220-3329_0a1f531e-55e6-7573-e063-6294a90aaa48
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SUS SCROFA BONE MARROW
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- BOIRON
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-01-08
- Substance
- SUS SCROFA BONE MARROW
- Active strength
- 8 [hp_X]/8[hp_X]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MEDULLA OSSIS SUIS
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUS SCROFA BONE MARROW | 8 [hp_X]/8[hp_X] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VP2CN2G7Y8 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-3329-41 | MEDULLA OSSIS SUIS | 8 [hp_X] in 1 TUBE | PELLET | 8 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-3329 | MEDULLA OSSIS SUIS (SUS SCROFA BONE MARROW) PELLET [BOIRON] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231115_61e659a2-f4af-42db-e053-2991aa0ab8f5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-3329-41 | 00220332941 | 8 [hp_X] in 1 TUBE (0220-3329-41) | 2018-01-08 | 0000-00-00 | No | No | Current |