0170 C
Pill imprint 0170 C has been identified as Oxaprozin 600 mg.
Oxaprozin 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.
Oxaprozin 600 mg is not subject to the Controlled Substances Act.
See also related documents.
Oxaprozin Images
- Imprint:
-
0170
C - Strength:
- 600 mg
- Color:
- Yellow
- Size:
- 19.00 mm
- Shape:
- Elliptical / Oval
- Availability:
- Prescription only
- Inactive Ingredients:
- corn starch
D&C Yellow No. 10
FD&C Yellow No. 6
hypromellose
lactose monohydrate
magnesium stearate
microcrystalline cellulose
polydextrose
polyethylene glycol
sodium starch glycolate type A potato
titanium dioxide
triacetin
- Drug Class:
- Nonsteroidal anti-inflammatory agents
- Pregnancy Category:
- C - Risk cannot be ruled out
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Dr. Reddy’s Laboratories Inc.
- National Drug Code (NDC):
- 55111-0170
| NDC Code | Manufacturer / Repackager |
|---|---|
| 66267-0407 | Nucare Pharmaceuticals Inc (repackager) |
| 68387-0180 | Keltman Pharmaceuticals Inc (repackager) |
| 63874-0353 | Altura Pharmaceuticals Inc (repackager) |
| 66336-0722 | Dispensing Solutions Inc. (repackager) |
| 23490-6047 | Palmetto State Pharmaceuticals Inc (repackager) |
Note: Inactive ingredients may vary.
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More Oxaprozin resources
- Oxaprozin (Wolters Kluwer)
- oxaprozin (Cerner Multum)
- oxaprozin (Micromedex) - Includes Dosage Information
- Oxaprozin (AHFS DI)
- Oxaprozin Potassium (AHFS DI)
- Daypro Alta (FDA)
- Oxaprozin (FDA)
- Oxaprozin Tablets (FDA)
- Oxaprozin (Wolters Kluwer)
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