Amitriptyline Hydrochloride NDC 71335-9710

Product information

Brand name (proprietary)

Amitriptyline Hydrochloride

Generic name (nonproprietary)

amitriptyline hydrochloride

Active ingredients

Amitriptyline hydrochloride — 150 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 213999

Marketing start

Feb 23, 2021

Listing expires

Dec 31, 2027

Identifiers

Product ID 71335-9710_e127fb06-d8b0-4db9-9fb5-8db4849b9ba6SPL ID e127fb06-d8b0-4db9-9fb5-8db4849b9ba6SPL set ID 9f9d6495-47ff-4dcf-9643-ebd5cd7499cbRxCUI 856773UNII 26LUD4JO9K

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

N471335971001 followed by a unit qualifier and the quantity Copy

Package 71335-9710-01. 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 213999

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