Package 0220-2799-41

Brand: kali iodatum

Generic: potassium iodide
NDC Package

Package Facts

Identity

Package NDC 0220-2799-41
Digits Only 0220279941
Product NDC 0220-2799
Description

6 [hp_C] in 1 TUBE (0220-2799-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand kali iodatum
Generic potassium iodide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e1685-b633-7e21-e063-6394a90a5324", "openfda": {"unii": ["1C4QK22F9J"], "spl_set_id": ["86075ed7-03be-0ded-e053-2a91aa0a2d84"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-2799-41)", "package_ndc": "0220-2799-41", "marketing_start_date": "19830303"}], "brand_name": "Kali iodatum", "product_id": "0220-2799_0a0e1685-b633-7e21-e063-6394a90a5324", "dosage_form": "PELLET", "product_ndc": "0220-2799", "generic_name": "POTASSIUM IODIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali iodatum", "active_ingredients": [{"name": "POTASSIUM IODIDE", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}