Package 0220-2582-41

Brand: hypericum perforatum

Generic: hypericum perforatum
NDC Package

Package Facts

Identity

Package NDC 0220-2582-41
Digits Only 0220258241
Product NDC 0220-2582
Description

200 [kp_C] in 1 TUBE (0220-2582-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand hypericum perforatum
Generic hypericum perforatum
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "476ac68b-041a-1698-e063-6294a90a7fdf", "openfda": {"unii": ["XK4IUX8MNB"], "spl_set_id": ["85cab607-c6b6-c28e-e053-2a91aa0adf57"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2582-41)", "package_ndc": "0220-2582-41", "marketing_start_date": "19830303"}], "brand_name": "Hypericum perforatum", "product_id": "0220-2582_476ac68b-041a-1698-e063-6294a90a7fdf", "dosage_form": "PELLET", "product_ndc": "0220-2582", "generic_name": "HYPERICUM PERFORATUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hypericum perforatum", "active_ingredients": [{"name": "HYPERICUM PERFORATUM", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20271231"}