NDC codes

FDA NDC Directory
Product NDC (as listed)51655-986Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51655-0986Add 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
51655-986-265165509862690 TABLET in 1 BOTTLE, PLASTIC (51655-986-26)Marketed from May 18, 2022
51655-986-525165509865230 TABLET in 1 BOTTLE, PLASTIC (51655-986-52)Marketed from May 18, 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
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071524
Marketing start
Listing expires
Identifiers
Product ID 51655-986_4a92b7c1-d0ac-e368-e063-6394a90a7c67SPL ID 4a92b7c1-d0ac-e368-e063-6394a90a7c67SPL set ID e07d7ee3-776d-1fa3-e053-2a95a90a7019RxCUI 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

N451655098626 followed by a unit qualifier and the quantity

Package 51655-0986-26. 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 071524

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

FDA NDC Directory listings under ANDA 071524
ProductStrengthForm · routeLabelerProduct NDC
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralREMEDYREPACK INC.70518-2973
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-530
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-537
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-424
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralTeva Pharmaceuticals USA, Inc.50111-561
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralAvKARE42291-869
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralProficient Rx LP71205-574
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8386

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