Package 44911-0209-1

Brand: aconite

Generic: aconitum napellus
NDC Package

Package Facts

Identity

Package NDC 44911-0209-1
Digits Only 4491102091
Product NDC 44911-0209
Description

30 mL in 1 BOTTLE, DROPPER (44911-0209-1)

Marketing

Marketing Status
Marketed Since 2015-07-15
Brand aconite
Generic aconitum napellus
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04259ae1-7e7d-4018-9866-9b0f378b2cfc", "openfda": {"unii": ["U0NQ8555JD"], "spl_set_id": ["e5f8aa8c-0764-49e8-a2b1-4b8291eef882"], "manufacturer_name": ["ENERGIQUE, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (44911-0209-1)", "package_ndc": "44911-0209-1", "marketing_start_date": "20150715"}], "brand_name": "ACONITE", "product_id": "44911-0209_04259ae1-7e7d-4018-9866-9b0f378b2cfc", "dosage_form": "LIQUID", "product_ndc": "44911-0209", "generic_name": "Aconitum napellus", "labeler_name": "ENERGIQUE, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACONITE", "active_ingredients": [{"name": "ACONITUM NAPELLUS WHOLE", "strength": "200 [hp_C]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20150715", "listing_expiration_date": "20261231"}