FDA.reportPublic FDA data

MAGNESIA PHOSPHORICA

Product NDC
0360-0265
Requested package NDC
0360-0265-02
11-digit product format
003600265
Labeler code
0360
Product ID
0360-0265_9ee13bac-d8ba-2cf0-e053-2995a90a810d
Type
HUMAN OTC DRUG
Nonproprietary name
MAGNESIA PHOS
Dosage form
TABLET
Route
SUBLINGUAL
Labeler
STANDARD HOMEOPATHIC COMPANY
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1997-02-17
Marketing end
0000-00-00
Substance
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength
6 [hp_X]/g
NDC exclude flag
No
Listing certified through
2021-12-31
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.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0360-02650360-0265-02DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0360-0265-02003600265021 g in 1 BOTTLE, PLASTIC (0360-0265-02) 1 g1997-02-170000-00-00NoNoCurrent