Doxepin Hydrochloride NDC 71335-2418

Product information

Brand name (proprietary)

Doxepin Hydrochloride

Generic name (nonproprietary)

doxepin hydrochloride

Active ingredients

Doxepin hydrochloride — 25 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 215113

Marketing start

Jun 27, 2022

Listing expires

Dec 31, 2026

Identifiers

Product ID 71335-2418_8885944d-8f69-4cc1-b92c-fa15777dcc43SPL ID 8885944d-8f69-4cc1-b92c-fa15777dcc43SPL set ID 13da67ec-370c-4647-8440-80fd55f1398eRxCUI 1000070UNII 3U9A0FE9N5

Pharmacologic class

Tricyclic Antidepressant

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

N471335241801 followed by a unit qualifier and the quantity Copy

Package 71335-2418-01. 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 215113

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