NDC 68788-7897 – Duloxetine Delayed-Release

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

Human Prescription Drug

Product NDC68788-7897

Product details

Brand name
Duloxetine Delayed-Release
Generic name
Duloxetine Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA203088
Marketed since
May 14, 2021
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (3)

Package NDCDescriptionSince
68788-7897-330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-3)May 14, 2021
68788-7897-660 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-6)May 14, 2021
68788-7897-990 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-9)May 14, 2021

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