NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1483Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1483Add 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
71335-1483-17133514830130 TABLET in 1 BOTTLE (71335-1483-1)Marketed from Jan 15, 2020
71335-1483-27133514830260 TABLET in 1 BOTTLE (71335-1483-2)Marketed from Mar 13, 2020
71335-1483-37133514830390 TABLET in 1 BOTTLE (71335-1483-3)Marketed from Aug 12, 2021
71335-1483-47133514830418 TABLET in 1 BOTTLE (71335-1483-4)Marketed from Feb 14, 2022
71335-1483-571335148305100 TABLET in 1 BOTTLE (71335-1483-5)Marketed from Feb 14, 2022
71335-1483-67133514830645 TABLET in 1 BOTTLE (71335-1483-6)Marketed from Feb 14, 2022
71335-1483-771335148307180 TABLET in 1 BOTTLE (71335-1483-7)Marketed from Feb 14, 2022

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 — 150 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206923
Marketing start
Listing expires
Identifiers
Product ID 71335-1483_31dfca90-1516-4b31-b377-bf8315419645SPL ID 31dfca90-1516-4b31-b377-bf8315419645SPL set ID 5605e909-dc75-4578-94c6-41bb96ba3e2aRxCUI 856364UNII 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

N471335148301 followed by a unit qualifier and the quantity

Package 71335-1483-01. 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 is 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 206923

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

FDA NDC Directory listings under ANDA 206923
ProductStrengthForm · routeLabelerProduct NDC
Trazodone HydrochlorideTrazodone hydrochloride 300 mg/1TabletOralAccord Healthcare, Inc.16729-302
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAccord Healthcare, Inc.16729-299
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralAccord Healthcare, Inc.16729-300
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralAccord Healthcare, Inc.16729-301
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralProficient Rx LP71205-630
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralBryant Ranch Prepack71335-1575

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