Package 0220-2139-41

Brand: formica rufa

Generic: formica rufa
NDC Package

Package Facts

Identity

Package NDC 0220-2139-41
Digits Only 0220213941
Product NDC 0220-2139
Description

30 [hp_C] in 1 TUBE (0220-2139-41)

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": "f19eb662-8f05-69f9-e053-2a95a90a7939", "openfda": {"unii": ["55H0W83JO5"], "spl_set_id": ["87377727-5cb1-23cc-e053-2a91aa0a9413"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2139-41)", "package_ndc": "0220-2139-41", "marketing_start_date": "19830303"}], "brand_name": "Formica rufa", "product_id": "0220-2139_f19eb662-8f05-69f9-e053-2a95a90a7939", "dosage_form": "PELLET", "product_ndc": "0220-2139", "generic_name": "FORMICA RUFA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Formica rufa", "active_ingredients": [{"name": "FORMICA RUFA", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}