Package 0220-0759-41

Brand: badiaga

Generic: spongilla lacustris
NDC Package

Package Facts

Identity

Package NDC 0220-0759-41
Digits Only 0220075941
Product NDC 0220-0759
Description

9 [hp_C] in 1 TUBE (0220-0759-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand badiaga
Generic spongilla lacustris
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09ba4ccf-6732-af53-e063-6294a90af1a8", "openfda": {"unii": ["6SZ0G98BHM"], "spl_set_id": ["84636dd0-8f8f-69ee-e053-2991aa0a7ed1"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-0759-41)", "package_ndc": "0220-0759-41", "marketing_start_date": "19830303"}], "brand_name": "Badiaga", "product_id": "0220-0759_09ba4ccf-6732-af53-e063-6294a90af1a8", "dosage_form": "PELLET", "product_ndc": "0220-0759", "generic_name": "SPONGILLA LACUSTRIS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Badiaga", "active_ingredients": [{"name": "SPONGILLA LACUSTRIS", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}