Duloxetine Delayed-Release (duloxetine hydrochloride) NDC 63629-1991

Product information

Brand name (proprietary)

Duloxetine Delayed-ReleaseSuffix: Delayed-Release

Generic name (nonproprietary)

duloxetine hydrochloride

Active ingredients

Duloxetine hydrochloride — 30 mg/1

Dosage form

Capsule, Delayed release pellets

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 203088

Marketing start

Jun 11, 2014

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 63629-1991_d5e81e01-e04b-4d91-b29e-96a346636a01SPL ID d5e81e01-e04b-4d91-b29e-96a346636a01SPL set ID ca36f94c-2215-436f-ada8-7319f4f3e054RxCUI 596930UNII 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

N463629199101 followed by a unit qualifier and the quantity Copy

Package 63629-1991-01. 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 203088

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

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