DAYPRO 13 81 (Daypro 600 mg)

Generic Name: oxaprozin

This pill with imprint "DAYPRO 13 81" is White, Elliptical / Oval and has been identified as Daypro 600 mg. It is manufactured by Pfizer U.S. Pharmaceuticals Group.

Daypro is used in the treatment of rheumatoid arthritis; osteoarthritis; juvenile rheumatoid arthritis and belongs to the drug class nonsteroidal anti-inflammatory agents. Risk cannot be ruled out during pregnancy. Daypro 600 mg is not a controlled substance under the Controlled Substance Act (CSA).

Daypro

Generic Name:

oxaprozin

Imprint:

DAYPRO 13 81

Strength:

600 mg

Color:

White

Size:

19.00 mm

Shape:

Elliptical / Oval

Availability:

Prescription only

Drug Class:

Nonsteroidal anti-inflammatory agents

Pregnancy Category:

C - Risk cannot be ruled out

CSA Schedule:

Not a controlled drug

Manufacturer:

Pfizer U.S. Pharmaceuticals Group

National Drug Code (NDC):

00025-1381

Inactive Ingredients:

microcrystalline cellulose
hypromelloses
methylcellulose (100 mPa.s)
magnesium stearate
polacrilin potassium
polyethylene glycol
titanium dioxide

Note: Inactive ingredients may vary.

Imprint Code FAQ's

Other Manufacturers / Repackagers:

NDC Code	Manufacturer / Repackager
59762-6002	Greenstone LLC
54569-3702	A-S Medication Solutions, LLC (repackager)
55289-0453	PDRX Pharmaceuticals Inc (repackager)
54868-2997	Physicians Total Care Inc (repackager)
52959-0252	H.J. Harkins Company, Inc (repackager)
66267-0065	Nucare Pharmaceuticals Inc (repackager)
49999-0072	Lake Erie Medical and Surgical Supply (repackager)

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