NDC 83209-721 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC83209-721

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Boswell Pharmacy Services LLC d/b/a BPS Wholesale
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
May 20, 2024
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (6)

Package NDCDescriptionSince
83209-721-066 CAPSULE in 1 BLISTER PACK (83209-721-06)May 20, 2024
83209-721-1010 CAPSULE in 1 BLISTER PACK (83209-721-10)May 20, 2024
83209-721-1515 CAPSULE in 1 BLISTER PACK (83209-721-15)May 20, 2024
83209-721-2020 CAPSULE in 1 BLISTER PACK (83209-721-20)May 20, 2024
83209-721-3030 CAPSULE in 1 BLISTER PACK (83209-721-30)May 20, 2024
83209-721-6060 CAPSULE in 1 BLISTER PACK (83209-721-60)May 20, 2024

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