DAYPRO 13 81 (Daypro 600 mg)

Generic Name: oxaprozin

Pill with imprint DAYPRO 13 81 is White, Capsule-shape and has been identified as Daypro 600 mg. It is supplied by Pfizer U.S. Pharmaceuticals Group.

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

Images for DAYPRO 13 81

Daypro

Generic Name: oxaprozin
Imprint: DAYPRO 13 81
Strength: 600 mg
Color: White
Size: 19.00 mm
Shape: Capsule-shape
Availability: Prescription only
Drug Class: Nonsteroidal anti-inflammatory drugs
Pregnancy Category: C - Risk cannot be ruled out
CSA Schedule: Not a controlled drug
Labeler / Supplier: Pfizer U.S. Pharmaceuticals Group
Inactive Ingredients: microcrystalline cellulose, methylcellulose (100 mPa.s), magnesium stearate, polacrilin potassium, titanium dioxide
Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code	Labeler / Repackager
00025-1381	Pfizer Inc.
59762-6002	Viatris
54569-3702	A-S Medication Solutions, LLC (repackager)
55289-0453	PDRX Pharmaceuticals Inc. (repackager)
54868-2997 (Discontinued)	Physicians Total Care Inc. (repackager)
52959-0252	H.J. Harkins Company, Inc. (repackager)
66267-0065 (Discontinued)	Nucare Pharmaceuticals Inc. (repackager)
49999-0072	Lake Erie Medical and Surgical Supply (repackager)