Lilly 3235 20mg (Duloxetine Hydrochloride Delayed-Release 20 mg)

Pill with imprint Lilly 3235 20mg is Green, Capsule-shape and has been identified as Duloxetine Hydrochloride Delayed-Release 20 mg. It is supplied by Prasco Laboratories.

Duloxetine is used in the treatment of chronic pain; back 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 Lilly 3235 20mg

Duloxetine hydrochloride delayed-release 20 mg Lilly 3235 20mg

Duloxetine Hydrochloride Delayed-Release

Imprint: Lilly 3235 20mg
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: Prasco Laboratories
Inactive Ingredients: gelatin, hypromelloses, hypromellose acetate succinate 16070722 (3 mm2/s), sodium lauryl sulfate, sucrose, magnesium silicate, titanium dioxide, triethyl citrate, FD&C Blue No. 2, ferric oxide yellow
Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code	Labeler / Repackager
66993-0075 (Discontinued)	Prasco Laboratories
00002-3235	Eli Lilly and Company
54868-5215 (Discontinued)	Physicians Total Care Inc. (repackager)
49999-0617	Lake Erie Medical and Surgical Supply (repackager)
33261-0742	Aidarex Pharmacuticals, LLC (repackager)