NDC codes

FDA NDC Directory
Product NDC (as listed)72789-079Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0079Add 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
72789-079-307278900793030 TABLET in 1 BOTTLE, PLASTIC (72789-079-30)Marketed from Apr 6, 2020

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 hydrochloride150 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071525
Marketing start
Listing expires
Identifiers
Product ID 72789-079_4019c854-3393-5b53-e063-6394a90abd16SPL ID 4019c854-3393-5b53-e063-6394a90abd16SPL set ID 9b022ae9-dd52-43ae-804b-ddf8e7cfd530RxCUI 856364UNII 6E8ZO8LRNMUPC 0372789079301
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

N472789007930 followed by a unit qualifier and the quantity

Package 72789-0079-30. 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 071525

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

FDA NDC Directory listings under ANDA 071525
ProductStrengthForm · routeLabelerProduct NDC
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8339
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralTeva Pharmaceuticals USA, Inc.50111-450
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralAvKARE42291-829

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