FDA.reportPublic FDA data

Magnesia phosphorica

Product NDC
71919-435
Requested package NDC
71919-435-10
11-digit product format
719190435
Labeler code
71919
Product ID
71919-435_7e576a9a-5318-06b5-e053-2a91aa0a87b5
Type
HUMAN OTC DRUG
Nonproprietary name
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-02-03
Marketing end
0000-00-00
Substance
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
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 packagepackage71919-43571919-435-10DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-435-1071919043510100 mL in 1 BOTTLE, GLASS (71919-435-10) 100 ml2010-02-030000-00-00NoNoCurrent