Package 63083-7140-1

Brand: thuja occidentalis 7140

Generic: thuja occidentalis
NDC Package

Package Facts

Identity

Package NDC 63083-7140-1
Digits Only 6308371401
Product NDC 63083-7140
Description

29.5 mL in 1 BOTTLE, DROPPER (63083-7140-1)

Marketing

Marketing Status
Marketed Since 1985-08-15
Brand thuja occidentalis 7140
Generic thuja occidentalis
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "94dc8bd9-ad89-4893-ad88-cd3bfcb2260a", "openfda": {"unii": ["0T0DQN8786"], "spl_set_id": ["11364528-399d-4f64-a682-ec8f503af0aa"], "manufacturer_name": ["Professional Complementary Health Formulas"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29.5 mL in 1 BOTTLE, DROPPER (63083-7140-1)", "package_ndc": "63083-7140-1", "marketing_start_date": "19850815"}], "brand_name": "Thuja occidentalis 7140", "product_id": "63083-7140_94dc8bd9-ad89-4893-ad88-cd3bfcb2260a", "dosage_form": "LIQUID", "product_ndc": "63083-7140", "generic_name": "Thuja occidentalis", "labeler_name": "Professional Complementary Health Formulas", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thuja occidentalis", "brand_name_suffix": "7140", "active_ingredients": [{"name": "THUJA OCCIDENTALIS LEAF", "strength": "6 [hp_X]/29.5mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19840815", "listing_expiration_date": "20271231"}