Register entry

Magnesium Products Inc.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
2
Live patents
0
Countries
1
Base
United States
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Magnesium Products, IncRegistrant: Magnesium Products Inc.5105 West 66th Street, Tulsa, Oklahoma (OK) 74131, United States (USA)Active ingredient (API) manufacture3009034868780532875
Catalogue

Drug listings by form and route

2

2 active NDC listings: 2 bulk ingredient. By marketing category: BULK INGREDIENT 2.

Dosage formNDCs
granule1
liquid1
RouteNDCs
Labeller name on the listingNDCs
magnesium products, inc.2
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
-Zinc Acetate Dihydrategranule72402-001BULK INGREDIENT
-Zinc Chloride Liquidliquid72402-002BULK INGREDIENT
Neighbours

Registered in the same town

2
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Comparable companies in United States

Enquiry

Common questions

Is Magnesium Products Inc. FDA approved?
Magnesium Products Inc. holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Magnesium Products Inc.'s drugs manufactured?
The FDA register lists Tulsa, OK. Registered operations: active ingredient (API) manufacture.
What drugs does Magnesium Products Inc. make?
2 products are listed under Magnesium Products Inc. in the openFDA NDC Directory, most often as granule; liquid. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.