NDC codes

FDA NDC Directory
Product NDC (as listed)67046-1540Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-1540Add 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 NDC11-digit (billing)PackageCopy
67046-1540-3670461540036704615400330 TABLET in 1 BLISTER PACK (67046-1540-3)Marketed from Mar 25, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Route
Oral
Labeler
Coupler LLCNDC labeler code 67046
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218988
Marketing start
Listing expires
Identifiers
Product ID 67046-1540_3135525b-d57b-06db-e063-6394a90adf5dSPL ID 3135525b-d57b-06db-e063-6394a90adf5dSPL set ID 31356804-951b-68c7-e063-6294a90a6410RxCUI 856373UNII 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

N467046154003 followed by a unit qualifier and the quantity

Package 67046-1540-03. 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 . 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 67046-1540

What is NDC 67046-1540?
67046-1540 is the product NDC for Trazodone Hydrochloride, Trazodone hydrochloride 100 mg/1 tablet, listed with the FDA by Coupler 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?
Coupler LLC, NDC labeler code 67046. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralAmerican Health Packaging60687-96560687-0965-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralREMEDYREPACK INC.70518-476070518-4760-0070518-4760-0270518-4760-03+1 more
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralNorthwind Health Company, LLC82868-11682868-0116-90
Trazodone HydrochlorideTrazodone hydrochloride 25 mg/1Tablet, Film coatedOralTRUPHARMA LLC52817-39552817-0395-10
Trazodone HydrochlorideTrazodone hydrochloride 75 mg/1Tablet, Film coatedOralTRUPHARMA LLC52817-39652817-0396-10
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralREMEDYREPACK INC.70518-473770518-4737-0070518-4737-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAmerican Health Packaging60687-95460687-0954-01
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralUnit Dose Solutions, Inc.87441-08087441-0080-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralUnit Dose Solutions, Inc.87441-08187441-0081-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1Tablet, Film coatedOralCoupler LLC67046-168467046-1684-03

All 158 Trazodone Hydrochloride NDCs

Other NDCs under ANDA 218988

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

FDA NDC Directory listings under ANDA 218988
ProductStrengthForm · routeLabelerProduct NDC
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralGolden State Medical Supply, Inc.51407-946
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralGolden State Medical Supply, Inc.51407-947
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralCoupler LLC67046-1506
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralGranules Pharmaceuticals Inc.70010-231
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralGranules Pharmaceuticals Inc.70010-232
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralGranules Pharmaceuticals Inc.70010-233
Trazodone HydrochlorideTrazodone hydrochloride 300 mg/1TabletOralGranules Pharmaceuticals Inc.70010-234
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralREMEDYREPACK INC.70518-4737
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralREMEDYREPACK INC.70518-4760
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralNorthwind Health Company, LLC82868-116
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralUnit Dose Solutions, Inc.87441-080

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