NDC 70247-012 – duloxetine

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

Human Prescription Drug

Product NDC70247-012

Product details

Brand name
duloxetine
Generic name
Duloxetine
Labeler
Qingdao BAHEAL Pharmaceutical Co., Ltd.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA210599
Marketed since
May 5, 2018
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 (1)

Package NDCDescriptionSince
70247-012-0660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-012-06)May 8, 2018

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