NDC 68180-997 – Fluoxetine Hydrochloride

Fluoxetine Hydrochloride 60 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68180-997

Product details

Brand name
Fluoxetine Hydrochloride
Generic name
Fluoxetine Hydrochloride
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211632
Marketed since
April 9, 2019
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68180-997-0630 TABLET in 1 BOTTLE (68180-997-06)Apr 9, 2019

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