MAGNESIA PHOSPHORICA
- Product NDC
- 60512-9152
- 11-digit product format
- 605129152
- Labeler code
- 60512
- Product ID
- 60512-9152_a5928f0b-b6e7-44af-a9ef-1196d1c7ab78
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MAGNESIA PHOSPHORICA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- HOMEOLAB USA INC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-11-30
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Active strength
- 1 [hp_X]/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60512-9152 | MAGNESIA PHOSPHORICA PELLET [HOMEOLAB USA INC] | 1 | Legacy NDC | 20111207_17e87337-5346-40a4-ad10-2c69eee144bf.zip |