Package 0220-1283-41

Brand: chelidonium majus

Generic: chelidonium majus
NDC Package

Package Facts

Identity

Package NDC 0220-1283-41
Digits Only 0220128341
Product NDC 0220-1283
Description

30 [hp_X] in 1 TUBE (0220-1283-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand chelidonium majus
Generic chelidonium majus
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09bf2450-da9b-ab38-e063-6294a90ab744", "openfda": {"unii": ["7E889U5RNN"], "spl_set_id": ["8528d6f7-b379-8c27-e053-2991aa0a88b2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-1283-41)", "package_ndc": "0220-1283-41", "marketing_start_date": "19830303"}], "brand_name": "Chelidonium majus", "product_id": "0220-1283_09bf2450-da9b-ab38-e063-6294a90ab744", "dosage_form": "PELLET", "product_ndc": "0220-1283", "generic_name": "CHELIDONIUM MAJUS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Chelidonium majus", "active_ingredients": [{"name": "CHELIDONIUM MAJUS", "strength": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}