NDC 47335-382 – Duloxetine

Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC47335-382

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090745
Marketed since
December 11, 2013
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (6)

Package NDCDescriptionSince
47335-382-08100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-08)Dec 11, 2013
47335-382-181000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-18)Dec 11, 2013
47335-382-61100 BLISTER PACK in 1 CARTON (47335-382-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACKDec 11, 2013
47335-382-8190 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-81)Dec 11, 2013
47335-382-8330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-83)Dec 11, 2013
47335-382-88100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-88)Dec 11, 2013

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