Package 0220-1761-41

Brand: digitalis purpurea

Generic: digitalis
NDC Package

Package Facts

Identity

Package NDC 0220-1761-41
Digits Only 0220176141
Product NDC 0220-1761
Description

200 [kp_C] in 1 TUBE (0220-1761-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand digitalis purpurea
Generic digitalis
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2f3b480-803e-331c-e053-2a95a90a745b", "openfda": {"unii": ["F1T8QT9U8B"], "spl_set_id": ["857b38d7-65fe-3ce2-e053-2a91aa0a7de9"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-1761-41)", "package_ndc": "0220-1761-41", "marketing_start_date": "19830303"}], "brand_name": "Digitalis purpurea", "product_id": "0220-1761_f2f3b480-803e-331c-e053-2a95a90a745b", "dosage_form": "PELLET", "product_ndc": "0220-1761", "generic_name": "DIGITALIS", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digitalis purpurea", "active_ingredients": [{"name": "DIGITALIS", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}