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TEVA 7542 (Duloxetine Hydrochloride Delayed-Release 20 mg)

Pill with imprint TEVA 7542 is Green, Capsule-shape and has been identified as Duloxetine Hydrochloride Delayed-Release 20 mg. It is supplied by Teva Pharmaceuticals USA Inc.

Duloxetine is used in the treatment of back pain; chronic pain; anxiety; depression; diabetic peripheral neuropathy and belongs to the drug class serotonin-norepinephrine reuptake inhibitors. Risk cannot be ruled out during pregnancy. Duloxetine 20 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for TEVA 7542

Duloxetine hydrochloride delayed-release 20 mg TEVA 7542
Duloxetine hydrochloride delayed-release 20 mg TEVA 7542
Duloxetine hydrochloride delayed-release 20 mg TEVA 7542
Duloxetine hydrochloride delayed-release 20 mg TEVA 7542

Duloxetine Hydrochloride Delayed-Release

Imprint
TEVA 7542
Strength
20 mg
Color
Green
Shape
Capsule-shape
Availability
Prescription only
Drug Class
Serotonin-norepinephrine reuptake inhibitors
Pregnancy Category
C - Risk cannot be ruled out
CSA Schedule
Not a controlled drug
Labeler / Supplier
Teva Pharmaceuticals USA Inc.
National Drug Code (NDC)
00093-7542 (Discontinued)
Inactive Ingredients
ferrosoferric oxide, silicon dioxide, gelatin, hypromellose 2910 (3 mPa.s), hypromellose 2910 (6 mPa.s), hypromellose phthalate (31% phthalate, 40 cst), lactose monohydrate, povidone k30, propylene glycol, shellac, sodium lauryl sulfate, sucrose, corn starch, magnesium silicate, titanium dioxide, triethyl citrate, D&C Yellow No. 10, FD&C Green No. 3, potassium hydroxide

Note: Inactive ingredients may vary.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.