Package 0220-2823-41

Brand: kali bromatum

Generic: potassium bromide
NDC Package

Package Facts

Identity

Package NDC 0220-2823-41
Digits Only 0220282341
Product NDC 0220-2823
Description

30 [hp_C] in 1 TUBE (0220-2823-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand kali bromatum
Generic potassium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f29293d0-8d4a-6fc8-e053-2995a90a0886", "openfda": {"unii": ["OSD78555ZM"], "spl_set_id": ["8517ac7c-8a4b-def4-e053-2991aa0a2fa0"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2823-41)", "package_ndc": "0220-2823-41", "marketing_start_date": "19830303"}], "brand_name": "Kali bromatum", "product_id": "0220-2823_f29293d0-8d4a-6fc8-e053-2995a90a0886", "dosage_form": "PELLET", "product_ndc": "0220-2823", "generic_name": "POTASSIUM BROMIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali bromatum", "active_ingredients": [{"name": "POTASSIUM BROMIDE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}