Package 0220-1847-41

Brand: echinacea angustifolia

Generic: echinacea angustifolia
NDC Package

Package Facts

Identity

Package NDC 0220-1847-41
Digits Only 0220184741
Product NDC 0220-1847
Description

6 [hp_X] in 1 TUBE (0220-1847-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand echinacea angustifolia
Generic echinacea angustifolia
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0cabf1-aac8-6492-e063-6294a90a8464", "openfda": {"unii": ["VB06AV5US8"], "spl_set_id": ["8590214e-e59a-8934-e053-2a91aa0a248b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_X] in 1 TUBE (0220-1847-41)", "package_ndc": "0220-1847-41", "marketing_start_date": "19830303"}], "brand_name": "Echinacea angustifolia", "product_id": "0220-1847_0a0cabf1-aac8-6492-e063-6294a90a8464", "dosage_form": "PELLET", "product_ndc": "0220-1847", "generic_name": "ECHINACEA ANGUSTIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Echinacea angustifolia", "active_ingredients": [{"name": "ECHINACEA ANGUSTIFOLIA", "strength": "6 [hp_X]/6[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}