digitalis purpurea
Generic: digitalis
Labeler: boironDrug Facts
Product Profile
Brand Name
digitalis purpurea
Generic Name
digitalis
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
digitalis 1 [hp_M]/[hp_M]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-1764
Product ID
0220-1764_0a0c7949-ae93-a51a-e063-6394a90a8a56
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1983-03-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02201764
Hyphenated Format
0220-1764
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
digitalis purpurea (source: ndc)
Generic Name
digitalis (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 [hp_M]/[hp_M]
Packaging
- 1 [hp_M] in 1 TUBE (0220-1764-41)
Packages (1)
Ingredients (1)
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"}