Register entryShortage reported

Oryza Pharmaceuticals, Inc.

Data as of · How to read this entry

Registered sites
0
Active NDC listings
22
Labeller names
4
Live patents
0
Shortage listings
5
Countries
0
Alert

Drug shortage listings

5
DrugPresentationStatusAvailabilityPosted / updated
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatryAmphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 5 mg; 5 mg; 5 mg; 5 mg (NDC 72516-012-01)CurrentUnavailable12 Oct 202216 Sept 2026
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatryAmphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 3.75 mg; 3.75 mg; 3.75 mg; 3.75 mg (NDC 72516-013-01)CurrentUnavailable12 Oct 202216 Sept 2026
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatryAmphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 7.5 mg; 7.5 mg; 7.5 mg; 7.5 mg (NDC 72516-011-01)CurrentUnavailable12 Oct 202216 Sept 2026
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatryAmphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 1.25 mg; 1.25 mg; 1.25 mg; 1.25 mg (NDC 72516-016-01)CurrentUnavailable12 Oct 202216 Sept 2026
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatryAmphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 2.5 mg; 2.5 mg; 2.5 mg; 2.5 mg (NDC 72516-014-01)CurrentUnavailable12 Oct 202216 Sept 2026
Catalogue

Drug listings by form and route

22

22 active NDC listings: 22 human prescription drug. By marketing category: ANDA 21, UNAPPROVED DRUG OTHER 1.

Dosage formNDCs
tablet, extended release12
tablet8
injection, solution1
powder, for suspension1
RouteNDCs
oral21
intravenous1
Labeller name on the listingNDCs
oryza pharmaceuticals inc.10
oryza pharmaceuticals inc.6
oryza pharmaceuticals, inc4
oryza pharmaceuticals, inc.2
Catalogue

Marketed products

22
BrandGeneric nameForm / routeNDC
Carbamazepine ERCarbamazepinetablet, extended release, oral72516-020ANDA
Carbamazepine ERCarbamazepinetablet, extended release, oral72516-021ANDA
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine SulfateDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfatetablet, oral72516-011ANDA
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine SulfateDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfatetablet, oral72516-012ANDA
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine SulfateDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfatetablet, oral72516-013ANDA
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine SulfateDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfatetablet, oral72516-014ANDA
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine SulfateDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfatetablet, oral72516-015ANDA
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine SulfateDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfatetablet, oral72516-016ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral72516-030ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral72516-031ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral72516-032ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral72516-033ANDA
Metoprolol succinateMetoprolol succinatetablet, extended release, oral72516-025ANDA
Metoprolol succinateMetoprolol succinatetablet, extended release, oral72516-026ANDA
Metoprolol succinateMetoprolol succinatetablet, extended release, oral72516-027ANDA
Metoprolol succinateMetoprolol succinatetablet, extended release, oral72516-028ANDA
Oseltamivir Phosphate for Oral SuspensionOseltamivir Phosphatepowder, for suspension, oral72516-029ANDA
Papaverine HydrochloridePapaverine Hydrochlorideinjection, solution, intravenous72516-024UNAPPROVED DRUG OTHER
TicagrelorTicagrelortablet, oral72516-017ANDA
TicagrelorTicagrelortablet, oral72516-018ANDA
buPropion Hydrochloride XLbupropion hydrochloridetablet, extended release, oral72516-035ANDA
buPropion Hydrochloride XLbupropion hydrochloridetablet, extended release, oral72516-036ANDA
Compare

Other companies listing dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate

Enquiry

Common questions

Is Oryza Pharmaceuticals, Inc. FDA approved?
Oryza Pharmaceuticals, Inc. holds no registered establishment of its own; 22 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Oryza Pharmaceuticals, Inc. make?
22 products are listed under Oryza Pharmaceuticals, Inc. in the openFDA NDC Directory, most often as tablet, extended release; tablet; injection, solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Are any Oryza Pharmaceuticals, Inc. products in shortage?
5 presentations are currently listed in the FDA drug shortage database under Oryza Pharmaceuticals, Inc., covering Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet.

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.