Package 76472-3039-1

Brand: thuja occidentalis 200ck

Generic: thuja occidentalis
NDC Package

Package Facts

Identity

Package NDC 76472-3039-1
Digits Only 7647230391
Product NDC 76472-3039
Description

80 PELLET in 1 CYLINDER (76472-3039-1)

Marketing

Marketing Status
Marketed Since 2011-11-23
Brand thuja occidentalis 200ck
Generic thuja occidentalis
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBLINGUAL"], "spl_id": "2dcc6766-0ad5-3099-e063-6394a90ae3cb", "openfda": {"upc": ["0810095311581"], "unii": ["19RAD88E6O"], "spl_set_id": ["cf8a98e7-ab41-bcc4-e053-2995a90ad8bd"], "manufacturer_name": ["SEVENE USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 CYLINDER (76472-3039-1)", "package_ndc": "76472-3039-1", "marketing_start_date": "20111123"}], "brand_name": "THUJA OCCIDENTALIS 200ck", "product_id": "76472-3039_2dcc6766-0ad5-3099-e063-6394a90ae3cb", "dosage_form": "PELLET", "product_ndc": "76472-3039", "generic_name": "THUJA OCCIDENTALIS", "labeler_name": "SEVENE USA", "product_type": "HUMAN OTC DRUG", "brand_name_base": "THUJA OCCIDENTALIS", "brand_name_suffix": "200ck", "active_ingredients": [{"name": "THUJA OCCIDENTALIS BARK", "strength": "200 [kp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20111123", "listing_expiration_date": "20261231"}