Package 0220-4611-41

Brand: scutellaria lateriflora

Generic: scutellaria lateriflora
NDC Package

Package Facts

Identity

Package NDC 0220-4611-41
Digits Only 0220461141
Product NDC 0220-4611
Product ID 0220-4611_0a24c4b8-4959-c2d4-e063-6294a90adfb2
Description

30 [hp_C] in 1 TUBE (0220-4611-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand scutellaria lateriflora
Generic scutellaria lateriflora
Sample Package No

Linked Drug Pages (1)

Scutellaria lateriflora ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a24c4b8-4959-c2d4-e063-6294a90adfb2", "openfda": {"unii": ["7BP4DH5PDC"], "spl_set_id": ["86cfeffd-8a17-2323-e053-2991aa0ace37"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-4611-41)", "package_ndc": "0220-4611-41", "marketing_start_date": "19830303"}], "brand_name": "Scutellaria lateriflora", "product_id": "0220-4611_0a24c4b8-4959-c2d4-e063-6294a90adfb2", "dosage_form": "PELLET", "product_ndc": "0220-4611", "generic_name": "SCUTELLARIA LATERIFLORA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Scutellaria lateriflora", "active_ingredients": [{"name": "SCUTELLARIA LATERIFLORA", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}