Package 0220-1359-41

Brand: cimifuga racemosa

Generic: black cohosh
NDC Package

Package Facts

Identity

Package NDC 0220-1359-41
Digits Only 0220135941
Product NDC 0220-1359
Description

30 [hp_C] in 1 TUBE (0220-1359-41)

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": "00efd7eb-9e04-7fbe-e063-6294a90affe6", "openfda": {"unii": ["K73E24S6X9"], "spl_set_id": ["852a9b35-1764-b1c7-e053-2a91aa0a7daf"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-1359-41)", "package_ndc": "0220-1359-41", "marketing_start_date": "19830303"}], "brand_name": "Cimifuga racemosa", "product_id": "0220-1359_00efd7eb-9e04-7fbe-e063-6294a90affe6", "dosage_form": "PELLET", "product_ndc": "0220-1359", "generic_name": "BLACK COHOSH", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cimifuga racemosa", "active_ingredients": [{"name": "BLACK COHOSH", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}