Package 0220-1346-41

Brand: cimifuga racemosa

Generic: black cohosh
NDC Package

Package Facts

Identity

Package NDC 0220-1346-41
Digits Only 0220134641
Product NDC 0220-1346
Description

5 [hp_C] in 1 TUBE (0220-1346-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand cimifuga racemosa
Generic black cohosh
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09bf3adf-99f8-6e40-e063-6394a90a1f45", "openfda": {"unii": ["K73E24S6X9"], "spl_set_id": ["8529e7f1-0c8e-ab5d-e053-2991aa0ab412"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 [hp_C] in 1 TUBE (0220-1346-41)", "package_ndc": "0220-1346-41", "marketing_start_date": "19830303"}], "brand_name": "Cimifuga racemosa", "product_id": "0220-1346_09bf3adf-99f8-6e40-e063-6394a90a1f45", "dosage_form": "PELLET", "product_ndc": "0220-1346", "generic_name": "BLACK COHOSH", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cimifuga racemosa", "active_ingredients": [{"name": "BLACK COHOSH", "strength": "5 [hp_C]/5[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}