NDC 31722-170 – Duloxetine

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

Human Prescription Drug

Product NDC31722-170

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA204343
Marketed since
December 30, 2020
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
31722-170-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-01)Dec 30, 2020
31722-170-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-10)Dec 30, 2020
31722-170-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-30)Dec 30, 2020
31722-170-317 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-170-31)Dec 30, 2020
31722-170-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-90)Jun 29, 2024

Other Duloxetine products