NDC codes

FDA NDC Directory
Product NDC (as listed)87441-081Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87441-0081Add 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
87441-081-018744100810130 TABLET in 1 BLISTER PACK (87441-081-01)Marketed from Jul 9, 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 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 87441-081_562ff53a-a14c-8b34-e063-6394a90ab16eSPL ID 562ff53a-a14c-8b34-e063-6394a90ab16eSPL set ID 562fdfb9-c060-63bc-e063-6294a90ad840RxCUI 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

N487441008101 followed by a unit qualifier and the quantity

Package 87441-0081-01. 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/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/1TabletOralNorthwind Health Company, LLC51655-366
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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