NDC 49252-009 – duloxetine

Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC49252-009

Product details

Brand name
duloxetine
Generic name
duloxetine
Labeler
Inventia Healthcare Limited.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202336
Marketed since
December 5, 2015
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 (5)

Package NDCDescriptionSince
49252-009-1030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-009-10)Dec 5, 2015
49252-009-1160 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-009-11)Dec 5, 2015
49252-009-1290 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-009-12)Dec 5, 2015
49252-009-181000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-009-18)Dec 5, 2015
49252-009-57100 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (49252-009-57)Dec 5, 2015

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