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93 948 (DICLOFENAC 50 mg)

Pill imprint 93 948 has been identified as Diclofenac potassium 50 mg.

Diclofenac is used in the treatment of back pain; ankylosing spondylitis; muscle pain; pain; frozen shoulder (and more), and belongs to the drug class nonsteroidal anti-inflammatory agents. There is positive evidence of human fetal risk during pregnancy. Diclofenac 50 mg is not a controlled substance under the Controlled Substance Act (CSA).

Diclofenac potassium 50 mg 93 948
Diclofenac potassium 50 mg 93 948
Diclofenac potassium 50 mg 93 948  Front
Diclofenac potassium 50 mg 93 948  Back
Diclofenac potassium
93 948
50 mg
8.00 mm
Prescription only
Drug Class:
Nonsteroidal anti-inflammatory agents
Pregnancy Category:
D - Positive evidence of risk
CSA Schedule:
Not a controlled drug
Teva Pharmaceuticals USA
National Drug Code (NDC):
Inactive Ingredients:
silicon dioxide
corn starch
FD&C Blue No. 2
FD&C Red No. 40
FD&C Yellow No. 6
lactose monohydrate
magnesium stearate
microcrystalline cellulose
polyethylene glycol 4000
sodium starch glycolate type A potato
titanium dioxide
tricalcium phosphate
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
54569-4770 A-S Medication Solutions, LLC (repackager)
52959-0659 H.J. Harkins Company, Inc (repackager)
68115-0101 Dispensexpress Inc (repackager)
16590-0072 Stat RX USA LLC (repackager)
57866-6920 Direct Dispensing Inc (repackager)
54868-5437 Physicians Total Care Inc (repackager)
58016-0444 Southwood Pharmaceuticals Inc (repackager)

Note: Inactive ingredients may vary.

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