Desipramine Hydrochloride NDC 45963-341

NDC codes

FDA NDC Directory

Product NDC (as listed)45963-341Labeler and product segments. Claims need a package NDC.

Product NDC at billing width45963-0341Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
45963-341-02	45963034102	100 TABLET, FILM COATED in 1 BOTTLE (45963-341-02)Marketed from May 9, 2006

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Desipramine Hydrochloride
Generic name (nonproprietary): desipramine hydrochloride
Active ingredients: Desipramine hydrochloride — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Actavis Pharma, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074430
Marketing start: May 9, 2006
Marketing end: Jul 31, 2027
Identifiers: Product ID 45963-341_b7478143-a6d3-4a43-ba49-63a8b422fa50SPL ID b7478143-a6d3-4a43-ba49-63a8b422fa50SPL set ID ba02a95d-d82e-4a13-90b4-a219abc0249aRxCUI 1099288, 1099292, 1099296, 1099300, 1099304, 1099316UNII 1Y58DO4MY1UPC 0345963345028, 0345963346506, 0345963344021, 0345963343024, 0345963341020
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

N445963034102 followed by a unit qualifier and the quantity

Package 45963-0341-02. 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

Current FDA label (SPL), effective Jul 1, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Desipramine hydrochloride tablets are indicated for the treatment of depression.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 074430

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

FDA NDC Directory listings under ANDA 074430
Product	Strength	Form · route	Labeler	Product NDC
Desipramine Hydrochloride	Desipramine hydrochloride 150 mg/1	Tablet, Film coatedOral	Actavis Pharma, Inc.	45963-346