Medication Guide App

93 670 (Gemfibrozil 600 mg)

Pill imprint 93 670 has been identified as Gemfibrozil 600 mg.

Gemfibrozil is used in the treatment of high cholesterol; hyperlipoproteinemia type iib, elevated ldl vldl; hyperlipoproteinemia; hyperlipoproteinemia type iv, elevated vldl; hyperlipoproteinemia type v, elevated chylomicrons vldl and belongs to the drug class fibric acid derivatives. Risk cannot be ruled out during pregnancy. Gemfibrozil 600 mg is not subject to the Controlled Substances Act.

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Images for 93 670 (Gemfibrozil 600 mg)

Gemfibrozil 600 mg 93 670  Front
Gemfibrozil 600 mg 93 670  Back
Gemfibrozil 600 mg 93 670
Gemfibrozil 600 mg 93 670
Gemfibrozil
Imprint:
93 670
Strength:
600 mg
Color:
White
Size:
19.00 mm
Shape:
Elliptical / Oval
Availability:
Prescription only
Drug Class:
Fibric acid derivatives
Pregnancy Category:
C - Risk cannot be ruled out
CSA Schedule:
N - Not a controlled drug
Manufacturer:
Teva Pharmaceuticals USA
National Drug Code (NDC):
00093-0670
Inactive Ingredients:
calcium stearate
silicon dioxide
hydroxypropyl cellulose
hypromellose 2910 (15 mPa.s)
microcrystalline cellulose
polydextrose
polyethylene glycol 4000
polysorbate 80
corn starch
titanium dioxide
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
51079-0787 UDL Laboratories Inc
00182-1956 Goldline Laboratories Inc
23490-5626 Palmetto State Pharmaceuticals Inc (repackager)
67544-0096 Prepak Systems Inc (repackager)
67544-0351 Prepak Systems Inc (repackager)
66336-0367 Dispensing Solutions Inc. (repackager)
68258-1067 Dispensing Solutions Inc. (repackager)
54868-2353 Physicians Total Care Inc (repackager)
49999-0114 Lake Erie Medical and Surgical Supply (repackager)
55289-0411 PDRX Pharmaceuticals Inc (repackager)

Note: Inactive ingredients may vary.

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