Package 0603-0209-22

Brand: magnesium oxide

Generic: magnesium oxide
NDC Package

Package Facts

Identity

Package NDC 0603-0209-22
Digits Only 0603020922
Product NDC 0603-0209
Description

120 TABLET in 1 BOTTLE (0603-0209-22)

Marketing

Marketing Status
Marketed Since 2014-07-01
Brand magnesium oxide
Generic magnesium oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f385cf62-d6c3-4072-a788-831e05f98638", "openfda": {"unii": ["3A3U0GI71G"], "rxcui": ["198741"], "spl_set_id": ["d3c5b01b-f0d6-4503-ab18-b1a72386e2c6"], "manufacturer_name": ["Endo USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (0603-0209-22)", "package_ndc": "0603-0209-22", "marketing_start_date": "20140701"}], "brand_name": "Magnesium Oxide", "product_id": "0603-0209_f385cf62-d6c3-4072-a788-831e05f98638", "dosage_form": "TABLET", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0603-0209", "generic_name": "Magnesium Oxide", "labeler_name": "Endo USA", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Magnesium Oxide", "active_ingredients": [{"name": "MAGNESIUM OXIDE", "strength": "400 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}