Nortriptyline Hydrochloride NDC 63629-3204

Product information

Brand name (proprietary)

Nortriptyline Hydrochloride

Generic name (nonproprietary)

nortriptyline hydrochloride

Active ingredients

Nortriptyline hydrochloride — 10 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 074132

Marketing start

Apr 5, 1995

Listing expires

Dec 31, 2026

Identifiers

Product ID 63629-3204_7d1dd83e-d7a4-4349-bcc8-a3e05aad53afSPL ID 7d1dd83e-d7a4-4349-bcc8-a3e05aad53afSPL set ID 43a81887-42b8-43b5-b58a-3f3df2e9949bRxCUI 198045UNII 00FN6IH15D

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

N463629320401 followed by a unit qualifier and the quantity Copy

Package 63629-3204-01. 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 074132

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