Package 0220-4813-41

Brand: sulphur

Generic: sulfur
NDC Package

Package Facts

Identity

Package NDC 0220-4813-41
Digits Only 0220481341
Product NDC 0220-4813
Description

200 [hp_X] in 1 TUBE (0220-4813-41)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "07ec81ae-f40a-15a2-e063-6394a90abacd", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["8695330d-2428-f590-e053-2a91aa0a86ba"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [hp_X] in 1 TUBE (0220-4813-41)", "package_ndc": "0220-4813-41", "marketing_start_date": "19830303"}], "brand_name": "Sulphur", "product_id": "0220-4813_07ec81ae-f40a-15a2-e063-6394a90abacd", "dosage_form": "PELLET", "product_ndc": "0220-4813", "generic_name": "SULFUR", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "200 [hp_X]/200[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}