Package 44911-0382-1

Brand: bryonia

Generic: bryonia (alba)
NDC Package

Package Facts

Identity

Package NDC 44911-0382-1
Digits Only 4491103821
Product NDC 44911-0382
Description

30 mL in 1 BOTTLE, DROPPER (44911-0382-1)

Marketing

Marketing Status
Marketed Since 2016-08-19
Brand bryonia
Generic bryonia (alba)
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5dfb385-847a-433b-a413-f8ad47616f8b", "openfda": {"upc": ["0363113600346"], "unii": ["T7J046YI2B"], "spl_set_id": ["f9a2b9f3-5e35-4c3a-a8ae-a7312118e4f0"], "manufacturer_name": ["Energique, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (44911-0382-1)", "package_ndc": "44911-0382-1", "marketing_start_date": "20160819"}], "brand_name": "Bryonia", "product_id": "44911-0382_b5dfb385-847a-433b-a413-f8ad47616f8b", "dosage_form": "LIQUID", "product_ndc": "44911-0382", "generic_name": "Bryonia (Alba)", "labeler_name": "Energique, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bryonia", "active_ingredients": [{"name": "BRYONIA ALBA ROOT", "strength": "200 [hp_C]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20160819", "listing_expiration_date": "20261231"}