GG 904
Pill imprint GG 904 has been identified as Diclofenac sodium XR 100 mg.
Diclofenac is used in the treatment of back pain; pain; osteoarthritis; sciatica; muscle pain (and more), and belongs to the drug class nonsteroidal anti-inflammatory agents. There is positive evidence of human fetal risk during pregnancy.
Diclofenac 100 mg is not subject to the Controlled Substances Act.
See also related documents.
Diclofenac sodium XR Images
- Imprint:
-
GG 904
- Strength:
- 100 mg
- Color:
- Brown
- Size:
- 9.00 mm
- Shape:
- Round
- Availability:
- Prescription only
- Inactive Ingredients:
- cetyl alcohol
hydroxypropyl cellulose
ferric oxide red
magnesium stearate
polyethylene glycol
povidone
silicon dioxide
sucrose
magnesium silicate
titanium dioxide
- Drug Class:
- Nonsteroidal anti-inflammatory agents
- Pregnancy Category:
- D - Positive evidence of risk
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Sandoz Pharmaceuticals Inc.
- National Drug Code (NDC):
- 00781-1381
| NDC Code | Manufacturer / Repackager |
|---|---|
| 54868-5011 | Physicians Total Care Inc (repackager) |
| 66267-0709 | Nucare Pharmaceuticals Inc (repackager) |
Note: Inactive ingredients may vary.
More Diclofenac Sodium XR resources
- Diclofenac
- Diclofenac (Wolters Kluwer)
- Diclofenac Enteric-Coated Tablets (Wolters Kluwer)
- Diclofenac Extended-Release Tablets (Wolters Kluwer)
- Diclofenac Immediate-Release Tablets (Wolters Kluwer)
- Diclofenac Potassium Powder Packets (Wolters Kluwer)
- diclofenac (Cerner Multum)
- diclofenac (Micromedex) - Includes Dosage Information
- Diclofenac Potassium (AHFS DI)
- Diclofenac Sodium (AHFS DI)
- diclofenac epolamine (AHFS DI)
- Diclofenac (FDA)
- Diclofenac Delayed Release Tablets (FDA)
- Diclofenac Extended Release Tablets 100mg (FDA)
- Diclofenac Potassium (FDA)
- Diclofenac Tablets (FDA)


