Duloxetine NDC 85534-0050

Product information

Brand name (proprietary)

Duloxetine

Generic name (nonproprietary)

duloxetine

Active ingredients

Duloxetine hydrochloride — 20 mg/1

Dosage form

Capsule, Delayed release pellets

Route

Oral

Labeler

HAWAII REPACK, INC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 090776

Marketing start

Dec 17, 2013

Listing expires

Dec 31, 2027

Other FDA classes

Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 85534-0050_5b0626a8-dcce-62ec-e063-6394a90abae5SPL ID 5b0626a8-dcce-62ec-e063-6394a90abae5SPL set ID b32a39d8-5f1a-4e44-bc46-b65925bde753RxCUI 596926, 596930, 596934UNII 9044SC542W

Pharmacologic class

Serotonin and Norepinephrine 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

N485534005000 followed by a unit qualifier and the quantity Copy

Package 85534-0050-00. 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 090776

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