Package 0220-1757-41

Brand: digitalis purpurea

Generic: digitalis
NDC Package

Package Facts

Identity

Package NDC 0220-1757-41
Digits Only 0220175741
Product NDC 0220-1757
Product ID 0220-1757_0a0c91f9-28b0-3d6d-e063-6294a90aec12
Description

30 [hp_C] in 1 TUBE (0220-1757-41)

Marketing

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

Linked Drug Pages (1)

Digitalis purpurea ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a0c91f9-28b0-3d6d-e063-6294a90aec12", "openfda": {"unii": ["F1T8QT9U8B"], "spl_set_id": ["857b018f-05d8-b040-e053-2991aa0a7321"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-1757-41)", "package_ndc": "0220-1757-41", "marketing_start_date": "19830303"}], "brand_name": "Digitalis purpurea", "product_id": "0220-1757_0a0c91f9-28b0-3d6d-e063-6294a90aec12", "dosage_form": "PELLET", "product_ndc": "0220-1757", "generic_name": "DIGITALIS", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digitalis purpurea", "active_ingredients": [{"name": "DIGITALIS", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}