NDC 55111-284 – Fluoxetine hydrochloride

Fluoxetine Hydrochloride 90 mg/1 · Capsule, Delayed Release Pellets · Oral

Human Prescription Drug

Product NDC55111-284

Product details

Brand name
Fluoxetine hydrochloride
Generic name
Fluoxetine Hydrochloride
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA078572
Marketed since
March 24, 2010
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
55111-284-481 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACKMar 24, 2010

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