Package 0220-3329-41

Brand: medulla ossis suis

Generic: sus scrofa bone marrow
NDC Package

Package Facts

Identity

Package NDC 0220-3329-41
Digits Only 0220332941
Product NDC 0220-3329
Product ID 0220-3329_0a1f531e-55e6-7573-e063-6294a90aaa48
Description

8 [hp_X] in 1 TUBE (0220-3329-41)

Marketing

Marketing Status
Marketed Since 2018-01-08
Brand medulla ossis suis
Generic sus scrofa bone marrow
Sample Package No

Linked Drug Pages (1)

MEDULLA OSSIS SUIS ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a1f531e-55e6-7573-e063-6294a90aaa48", "openfda": {"unii": ["VP2CN2G7Y8"], "spl_set_id": ["61e659a2-f4af-42db-e053-2991aa0ab8f5"], "manufacturer_name": ["BOIRON"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 [hp_X] in 1 TUBE (0220-3329-41)", "package_ndc": "0220-3329-41", "marketing_start_date": "20180108"}], "brand_name": "MEDULLA OSSIS SUIS", "product_id": "0220-3329_0a1f531e-55e6-7573-e063-6294a90aaa48", "dosage_form": "PELLET", "product_ndc": "0220-3329", "generic_name": "SUS SCROFA BONE MARROW", "labeler_name": "BOIRON", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MEDULLA OSSIS SUIS", "active_ingredients": [{"name": "SUS SCROFA BONE MARROW", "strength": "8 [hp_X]/8[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20180108", "listing_expiration_date": "20261231"}