Package 0220-0349-41

Brand: antimonium crudum

Generic: antimony trisulfide
NDC Package

Package Facts

Identity

Package NDC 0220-0349-41
Digits Only 0220034941
Product NDC 0220-0349
Description

12 [hp_C] in 1 TUBE (0220-0349-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand antimonium crudum
Generic antimony trisulfide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d080f65-ec7d-0315-e063-6394a90ad441", "openfda": {"unii": ["F79059A38U"], "spl_set_id": ["845f0616-618c-b769-e053-2a91aa0ab8aa"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_C] in 1 TUBE (0220-0349-41)", "package_ndc": "0220-0349-41", "marketing_start_date": "19830303"}], "brand_name": "Antimonium crudum", "product_id": "0220-0349_0d080f65-ec7d-0315-e063-6394a90ad441", "dosage_form": "PELLET", "product_ndc": "0220-0349", "generic_name": "ANTIMONY TRISULFIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antimonium crudum", "active_ingredients": [{"name": "ANTIMONY TRISULFIDE", "strength": "12 [hp_C]/12[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}