Package 0220-1764-41

Brand: digitalis purpurea

Generic: digitalis
NDC Package

Package Facts

Identity

Package NDC 0220-1764-41
Digits Only 0220176441
Product NDC 0220-1764
Description

1 [hp_M] in 1 TUBE (0220-1764-41)

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": "0a0c7949-ae93-a51a-e063-6394a90a8a56", "openfda": {"unii": ["F1T8QT9U8B"], "spl_set_id": ["857b3951-c4e1-b042-e053-2991aa0aafb2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-1764-41)", "package_ndc": "0220-1764-41", "marketing_start_date": "19830303"}], "brand_name": "Digitalis purpurea", "product_id": "0220-1764_0a0c7949-ae93-a51a-e063-6394a90a8a56", "dosage_form": "PELLET", "product_ndc": "0220-1764", "generic_name": "DIGITALIS", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digitalis purpurea", "active_ingredients": [{"name": "DIGITALIS", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}