magnesium oxide

Generic: magnesium oxide

Labeler: endo usa
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name magnesium oxide
Generic Name magnesium oxide
Labeler endo usa
Dosage Form TABLET
Routes
ORAL
Active Ingredients

magnesium oxide 400 mg/1

Manufacturer
Endo USA

Identifiers & Regulatory

Product NDC 0603-0209
Product ID 0603-0209_f385cf62-d6c3-4072-a788-831e05f98638
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2014-07-01

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06030209
Hyphenated Format 0603-0209

Supplemental Identifiers

RxCUI
198741
UNII
3A3U0GI71G

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name magnesium oxide (source: ndc)
Generic Name magnesium oxide (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (0603-0209-22)
source: ndc

Packages (1)

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

Ingredients (1)

magnesium oxide (400 mg/1)

Linked Drug Pages (1)

Magnesium Oxide ndc-match (0.9)

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"}