Home NDC 0220-3329 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 UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination VP2CN2G7Y8 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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