NDC 50771-203 – Duloxetine Hydrochloride

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

Human Prescription Drug

Product NDC50771-203

Product details

Brand name
Duloxetine Hydrochloride
Generic name
Duloxetine Hydrochloride
Labeler
Yaopharma Co., Ltd.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA207219
Marketed since
January 1, 2024
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
50771-203-0130 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-01)Jan 1, 2024
50771-203-02500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-02)Jan 1, 2024

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