What is NDC 52817-395?

52817-395 is the product NDC for Trazodone Hydrochloride, Trazodone hydrochloride 25 mg/1 tablet, film coated, listed with the FDA by TRUPHARMA LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

TRUPHARMA LLC, NDC labeler code 52817. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Trazodone Hydrochloride?

157 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Trazodone Hydrochloride NDC 52817-395

NDC codes

FDA NDC Directory

Product NDC (as listed)52817-395Labeler and product segments. Claims need a package NDC.

Product NDC at billing width52817-0395Add 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
52817-395-10	5281703951052817039510	100 TABLET, FILM COATED in 1 BOTTLE (52817-395-10)Marketed from Sep 3, 2026

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 — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: TRUPHARMA LLCNDC labeler code 52817
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 072193
Marketing start: Sep 3, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 52817-395_203c92fc-3666-44b8-b89c-0b1acf94f137SPL ID 203c92fc-3666-44b8-b89c-0b1acf94f137SPL set ID a57da4f8-151d-4a74-8710-6158d1da3852RxCUI 2751852, 2751854UNII 6E8ZO8LRNM
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

N452817039510 followed by a unit qualifier and the quantity

Package 52817-0395-10. 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 Sep 3, 2026. 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)

About NDC 52817-395

What is NDC 52817-395?: 52817-395 is the product NDC for Trazodone Hydrochloride, Trazodone hydrochloride 25 mg/1 tablet, film coated, listed with the FDA by TRUPHARMA LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Trazodone Hydrochloride.
What is the active ingredient?: Trazodone hydrochloride.
Who is the labeler?: TRUPHARMA LLC, NDC labeler code 52817. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Trazodone Hydrochloride?: 157 other product NDCs are listed under this name. See all Trazodone Hydrochloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Trazodone Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Trazodone Hydrochloride	Trazodone hydrochloride 100 mg/1	TabletOral	American Health Packaging	60687-965	60687-0965-01
Trazodone Hydrochloride	Trazodone hydrochloride 50 mg/1	TabletOral	REMEDYREPACK INC.	70518-4760	70518-4760-0070518-4760-0270518-4760-03+1 more
Trazodone Hydrochloride	Trazodone hydrochloride 100 mg/1	TabletOral	Northwind Health Company, LLC	82868-116	82868-0116-90
Trazodone Hydrochloride	Trazodone hydrochloride 75 mg/1	Tablet, Film coatedOral	TRUPHARMA LLC	52817-396	52817-0396-10
Trazodone Hydrochloride	Trazodone hydrochloride 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-4737	70518-4737-0070518-4737-01
Trazodone Hydrochloride	Trazodone hydrochloride 50 mg/1	TabletOral	American Health Packaging	60687-954	60687-0954-01
Trazodone Hydrochloride	Trazodone hydrochloride 100 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-080	87441-0080-01
Trazodone Hydrochloride	Trazodone hydrochloride 50 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-081	87441-0081-01
Trazodone Hydrochloride	Trazodone hydrochloride 50 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1684	67046-1684-03
Trazodone Hydrochloride	Trazodone hydrochloride 150 mg/1	TabletOral	REMEDYREPACK INC.	70518-4690	70518-4690-00

All 158 Trazodone Hydrochloride NDCs

Other NDCs under ANDA 072193

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

FDA NDC Directory listings under ANDA 072193
Product	Strength	Form · route	Labeler	Product NDC
Trazodone Hydrochloride	Trazodone hydrochloride 75 mg/1	Tablet, Film coatedOral	TRUPHARMA LLC	52817-396
Trazodone Hydrochloride	Trazodone hydrochloride 100 mg/1	Tablet, Film coatedOral	Oxford Pharmaceuticals, LLC	69584-885