Magnesium Oxide
- Product NDC
- 63629-2217
- 11-digit product format
- 636292217
- Labeler code
- 63629
- Product ID
- 63629-2217_9be44461-e1a6-48f3-83e9-41576729aa7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Magnesium Oxide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-11-10
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM OXIDE
- Active strength
- 253 mg/1
- Pharmacologic 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]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2217-1 | 63629221701 | 100 TABLET in 1 BOTTLE (63629-2217-1) | 100 tablet | 2021-05-19 | 0000-00-00 | No | No | Current |