Package 0220-1767-41

Brand: digitalis purpurea

Generic: digitalis
NDC Package

Package Facts

Identity

Package NDC 0220-1767-41
Digits Only 0220176741
Product NDC 0220-1767
Product ID 0220-1767_0a0c9b00-4174-3584-e063-6294a90ae21c
Description

6 [hp_X] in 1 TUBE (0220-1767-41)

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": "0a0c9b00-4174-3584-e063-6294a90ae21c", "openfda": {"unii": ["UD4O8TY7RW"], "spl_set_id": ["6854ecc7-b3bf-b30e-e053-2a91aa0a84f4"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_X] in 1 TUBE (0220-1767-41)", "package_ndc": "0220-1767-41", "marketing_start_date": "19830303"}], "brand_name": "Digitalis purpurea", "product_id": "0220-1767_0a0c9b00-4174-3584-e063-6294a90ae21c", "dosage_form": "PELLET", "product_ndc": "0220-1767", "generic_name": "DIGITALIS", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digitalis purpurea", "active_ingredients": [{"name": "DIGITALIS PURPUREA WHOLE", "strength": "6 [hp_X]/6[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}