NDC 63187-702 – Duloxetine Delayed-release

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

Human Prescription Drug

Product NDC63187-702

Product details

Brand name
Duloxetine Delayed-release
Generic name
Duloxetine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA203088
Marketed since
June 11, 2014
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 (3)

Package NDCDescriptionSince
63187-702-3030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-30)May 2, 2016
63187-702-6060 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-60)May 2, 2016
63187-702-9090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-90)May 2, 2016

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