NDC 68645-130 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC68645-130

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Legacy Pharmaceutical Packaging, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA076001
Marketed since
January 25, 2011
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
68645-130-5430 CAPSULE in 1 BOTTLE (68645-130-54)Jan 25, 2011

Recalls mentioning this NDC

Other Fluoxetine products