MAGNESIA PHOSPHORICA
- Product NDC
- 71919-744
- 11-digit product format
- 719190744
- Labeler code
- 71919
- Product ID
- 71919-744_6dcab3fe-c0f0-ffa9-e053-2a91aa0a98ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Washington Homeopathic Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-05-31
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Active strength
- 6 [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 71919-744 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 71919-744 | 71919-744-36 | D | Discontinued by firm | 2026-07-31 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71919-744-36 | 2022-03-25 | C162847 | 48780-1 | 9d75b9cf-facd-f424-e053-dadaa90a57ce | MAGNESIA PHOSPHORICA |
| 71919-744-36 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-facd-f424-e053-dadaa90a57ce | MAGNESIA PHOSPHORICA |