Package 0220-2140-41

Brand: formica rufa

Generic: formica rufa
NDC Package

Package Facts

Identity

Package NDC 0220-2140-41
Digits Only 0220214041
Product NDC 0220-2140
Description

200 [kp_C] in 1 TUBE (0220-2140-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand formica rufa
Generic formica rufa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0cd0a0-f2ca-c28b-e063-6394a90ac393", "openfda": {"unii": ["55H0W83JO5"], "spl_set_id": ["85a14970-41be-0612-e053-2a91aa0ab023"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2140-41)", "package_ndc": "0220-2140-41", "marketing_start_date": "19830303"}], "brand_name": "Formica rufa", "product_id": "0220-2140_0a0cd0a0-f2ca-c28b-e063-6394a90ac393", "dosage_form": "PELLET", "product_ndc": "0220-2140", "generic_name": "FORMICA RUFA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Formica rufa", "active_ingredients": [{"name": "FORMICA RUFA", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}