Magnesium Oxide
- Product NDC
- 10135-583
- 11-digit product format
- 101350583
- Labeler code
- 10135
- Product ID
- 10135-583_096293fe-3cc5-4c19-94c2-48d82872f023
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Magnesium Oxide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals Inc
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-02-01
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM OXIDE
- Active strength
- 400 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10135-583-62 | Magnesium Oxide | 120 in 1 BOTTLE | TABLET | 120 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10135-583 | MAGNESIUM OXIDE TABLET [MARLEX PHARMACEUTICALS INC] | 1 | Legacy NDC, 1 package rows | 20190206_ca0c1df9-1285-4131-99e8-4198adda3341.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10135-583-62 | 10135058362 | 120 in 1 BOTTLE | Historical |