Package 0220-4820-41
Brand: sulphur
Generic: sulfurPackage Facts
Identity
Package NDC
0220-4820-41
Digits Only
0220482041
Product NDC
0220-4820
Description
1 [hp_M] in 1 TUBE (0220-4820-41)
Marketing
Marketing Status
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": "f52c0d73-6bd9-6378-e053-2995a90aebc1", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["8696b1c1-7329-3eed-e053-2991aa0a9617"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-4820-41)", "package_ndc": "0220-4820-41", "marketing_start_date": "19830303"}], "brand_name": "Sulphur", "product_id": "0220-4820_f52c0d73-6bd9-6378-e053-2995a90aebc1", "dosage_form": "PELLET", "product_ndc": "0220-4820", "generic_name": "SULFUR", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}