NDC codes

FDA NDC Directory
Product NDC (as listed)51655-366Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51655-0366Add 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
51655-366-265165503662690 TABLET in 1 BOTTLE, PLASTIC (51655-366-26)Marketed from Jan 5, 2023
51655-366-525165503665230 TABLET in 1 BOTTLE, PLASTIC (51655-366-52)Marketed from Nov 30, 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 hydrochloride50 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071523
Marketing start
Listing expires
Identifiers
Product ID 51655-366_49daf198-ebf2-ddd1-e063-6394a90a54d7SPL ID 49daf198-ebf2-ddd1-e063-6394a90a54d7SPL set ID f2f2290f-b53c-3b38-e053-2995a90a157dRxCUI 856377UNII 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

N451655036626 followed by a unit qualifier and the quantity

Package 51655-0366-26. 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)

Other NDCs under ANDA 071523

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

FDA NDC Directory listings under ANDA 071523
ProductStrengthForm · routeLabelerProduct NDC
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-529
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-525
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralUnit Dose Solutions, Inc.87441-081
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8371
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralTeva Pharmaceuticals USA, Inc.50111-560
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralProficient Rx LP71205-568
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAvKARE42291-868
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralREMEDYREPACK INC.70518-2929

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