Package 0220-2556-41

Brand: hydrastis canadensis

Generic: goldenseal
NDC Package

Package Facts

Identity

Package NDC 0220-2556-41
Digits Only 0220255641
Product NDC 0220-2556
Description

200 [kp_C] in 1 TUBE (0220-2556-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand hydrastis canadensis
Generic goldenseal
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d09c701-75d7-1f98-e063-6294a90ad44a", "openfda": {"unii": ["ZW3Z11D0JV"], "spl_set_id": ["85ba256f-20eb-2f8e-e053-2a91aa0a308f"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2556-41)", "package_ndc": "0220-2556-41", "marketing_start_date": "19830303"}], "brand_name": "Hydrastis canadensis", "product_id": "0220-2556_0d09c701-75d7-1f98-e063-6294a90ad44a", "dosage_form": "PELLET", "product_ndc": "0220-2556", "generic_name": "GOLDENSEAL", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hydrastis canadensis", "active_ingredients": [{"name": "GOLDENSEAL", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}