Package 0220-4839-41

Brand: sulphur iodatum

Generic: sulfur iodide
NDC Package

Package Facts

Identity

Package NDC 0220-4839-41
Digits Only 0220483941
Product NDC 0220-4839
Product ID 0220-4839_0a3421ae-8d23-3d0b-e063-6394a90ad467
Description

200 [kp_C] in 1 TUBE (0220-4839-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand sulphur iodatum
Generic sulfur iodide
Sample Package No

Linked Drug Pages (1)

SULPHUR IODATUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a3421ae-8d23-3d0b-e063-6394a90ad467", "openfda": {"unii": ["L6L8KA2AA0"], "spl_set_id": ["86935e36-ab98-b8d1-e053-2a91aa0ab0b6"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-4839-41)", "package_ndc": "0220-4839-41", "marketing_start_date": "19830303"}], "brand_name": "SULPHUR IODATUM", "product_id": "0220-4839_0a3421ae-8d23-3d0b-e063-6394a90ad467", "dosage_form": "PELLET", "product_ndc": "0220-4839", "generic_name": "SULFUR IODIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SULPHUR IODATUM", "active_ingredients": [{"name": "SULFUR IODIDE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}