Package 0220-4830-41

Brand: sulphur

Generic: sulfur
NDC Package

Package Facts

Identity

Package NDC 0220-4830-41
Digits Only 0220483041
Product NDC 0220-4830
Description

30 [hp_C] in 1 TUBE (0220-4830-41)

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": "f67ce46f-fe86-e06f-e053-2a95a90ae28d", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["869735c4-f8d6-1b5b-e053-2a91aa0a5920"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-4830-41)", "package_ndc": "0220-4830-41", "marketing_start_date": "19830303"}], "brand_name": "Sulphur", "product_id": "0220-4830_f67ce46f-fe86-e06f-e053-2a95a90ae28d", "dosage_form": "PELLET", "product_ndc": "0220-4830", "generic_name": "SULFUR", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}