DAYPRO 13 81 (Daypro 600 mg)
Generic Name: oxaprozin
Pill imprint DAYPRO 13 81 has been identified as Daypro 600 mg.
Daypro is used in the treatment of osteoarthritis; rheumatoid arthritis; 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).
- 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
| 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) |
| 55045-2120 | Dispensing Solutions Inc. (repackager) |
| 66267-0065 | Nucare Pharmaceuticals Inc (repackager) |
| 49999-0072 | Lake Erie Medical and Surgical Supply (repackager) |
Note: Inactive ingredients may vary.
More about Daypro (oxaprozin)
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Disclaimer:
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