NDC 33342-160 – Duloxetine Hydrochloride

Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC33342-160

Product details

Brand name
Duloxetine Hydrochloride
Generic name
Duloxetine Hydrochloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA204815
Marketed since
March 24, 2017
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
33342-160-0960 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-09)Mar 24, 2017
33342-160-1090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-10)Mar 24, 2017
33342-160-1210 BLISTER PACK in 1 CARTON (33342-160-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACKMar 24, 2017
33342-160-441000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-44)Mar 24, 2017

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