Package 0220-3796-41

Brand: onosmodium virginianum

Generic: onosmodium virginianum
NDC Package

Package Facts

Identity

Package NDC 0220-3796-41
Digits Only 0220379641
Product NDC 0220-3796
Description

30 [hp_C] in 1 TUBE (0220-3796-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand onosmodium virginianum
Generic onosmodium virginianum
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a2107cc-30c4-4bb8-e063-6394a90a9181", "openfda": {"unii": ["604NK4250S"], "spl_set_id": ["690808cf-72ca-5857-e053-2991aa0ab8c4"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-3796-41)", "package_ndc": "0220-3796-41", "marketing_start_date": "19830303"}], "brand_name": "Onosmodium virginianum", "product_id": "0220-3796_0a2107cc-30c4-4bb8-e063-6394a90a9181", "dosage_form": "PELLET", "product_ndc": "0220-3796", "generic_name": "ONOSMODIUM VIRGINIANUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Onosmodium virginianum", "active_ingredients": [{"name": "ONOSMODIUM VIRGINIANUM", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}