Fluoxetine (fluoxetine hydrochloride) NDC 71335-2020

Product information

Brand name (proprietary)

Fluoxetine

Generic name (nonproprietary)

fluoxetine hydrochloride

Active ingredients

Fluoxetine hydrochloride — 20 mg/1

Dosage form

Capsule

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 204597

Marketing start

Mar 16, 2015

Listing expires

Dec 31, 2026

Other FDA classes

Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 71335-2020_c282532b-eca5-434b-8101-34f75853cc3bSPL ID c282532b-eca5-434b-8101-34f75853cc3bSPL set ID 3d5d03ff-0d0c-429f-b747-31ff3465d39dRxCUI 310385UNII I9W7N6B1KJ

Pharmacologic class

Serotonin Reuptake Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335202001 followed by a unit qualifier and the quantity Copy

Package 71335-2020-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 204597

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

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