Trazodone Hydrochloride NDC 57664-026

NDC codes

FDA NDC Directory

Product NDC (as listed)57664-026Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57664-0026Add 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
57664-026-72	57664002672	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-026-72)Marketed from Oct 3, 2022
57664-026-74	57664002674	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-026-74)Marketed from Oct 3, 2022
57664-026-75	57664002675	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-026-75)Marketed from Oct 3, 2022

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): Trazodone Hydrochloride
Generic name (nonproprietary): trazodone hydrochloride
Active ingredients: Trazodone hydrochloride — 100 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 073137
Marketing start: Oct 3, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 57664-026_323e3d63-4d8d-7088-e063-6294a90abb0fSPL ID 323e3d63-4d8d-7088-e063-6294a90abb0fSPL set ID f291b905-a739-5e43-e053-2995a90ac40cRxCUI 856364, 856373, 856377UNII 6E8ZO8LRNMUPC 0357664014721
Pharmacologic class: Serotonin 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

N457664002672 followed by a unit qualifier and the quantity

Package 57664-0026-72. 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 Apr 8, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Trazodone hydrochloride tablets are indicated for the treatment of major depressive disorder (MDD) in adults. Trazodone hydrochloride tablets are a selective serotonin reuptake inhibitor indicated for the treatment of major depressive disorder (MDD) ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 073137

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

FDA NDC Directory listings under ANDA 073137
Product	Strength	Form · route	Labeler	Product NDC
Trazodone Hydrochloride	Trazodone hydrochloride 100 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1662
Trazodone Hydrochloride	Trazodone hydrochloride 50 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1684
Trazodone Hydrochloride	Trazodone hydrochloride 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4363
Trazodone Hydrochloride	Trazodone hydrochloride 50 mg/1	Tablet, Film coatedOral	Sun Pharmaceutical Industries, Inc.	57664-014
Trazodone Hydrochloride	Trazodone hydrochloride 150 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	57664-053