Package 44911-0166-1

Brand: kali mur

Generic: kali muriaticum
NDC Package

Package Facts

Identity

Package NDC 44911-0166-1
Digits Only 4491101661
Product NDC 44911-0166
Description

30 mL in 1 BOTTLE, DROPPER (44911-0166-1)

Marketing

Marketing Status
Marketed Since 2015-05-20
Brand kali mur
Generic kali muriaticum
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e0456aa8-e11c-4b9c-8e0a-32cae2d40afd", "openfda": {"unii": ["660YQ98I10"], "spl_set_id": ["db9894e6-2de0-428e-b553-11bb39a1d711"], "manufacturer_name": ["Energique, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (44911-0166-1)", "package_ndc": "44911-0166-1", "marketing_start_date": "20150520"}], "brand_name": "Kali Mur", "product_id": "44911-0166_e0456aa8-e11c-4b9c-8e0a-32cae2d40afd", "dosage_form": "LIQUID", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "44911-0166", "generic_name": "Kali Muriaticum", "labeler_name": "Energique, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali Mur", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "200 [hp_C]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20150520", "listing_expiration_date": "20261231"}