Package 44911-0156-1

Brand: thuja

Generic: thuja occidentalis
NDC Package

Package Facts

Identity

Package NDC 44911-0156-1
Digits Only 4491101561
Product NDC 44911-0156
Product ID 44911-0156_4906610c-6c3c-4086-80f1-08f49052811b
Description

30 mL in 1 BOTTLE, DROPPER (44911-0156-1)

Marketing

Marketing Status
Discontinued 2026-06-11
Brand thuja
Generic thuja occidentalis
Sample Package No

Linked Drug Pages (1)

Thuja ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4906610c-6c3c-4086-80f1-08f49052811b", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["25ec51fc-c898-4cbc-a579-57c5e9514a34"], "manufacturer_name": ["Energique, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (44911-0156-1)", "package_ndc": "44911-0156-1", "marketing_end_date": "20260611", "marketing_start_date": "20150514"}], "brand_name": "Thuja", "product_id": "44911-0156_4906610c-6c3c-4086-80f1-08f49052811b", "dosage_form": "LIQUID", "product_ndc": "44911-0156", "generic_name": "Thuja Occidentalis", "labeler_name": "Energique, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thuja", "active_ingredients": [{"name": "THUJA OCCIDENTALIS LEAFY TWIG", "strength": "30 [hp_C]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_end_date": "20260611", "marketing_start_date": "20150514"}