NDC codes

FDA NDC Directory
Product NDC (as listed)0615-8371Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-8371Add 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
0615-8371-050061583710515 TABLET in 1 BLISTER PACK (0615-8371-05)Marketed from Feb 11, 2022
0615-8371-07006158371077 TABLET in 1 BLISTER PACK (0615-8371-07)Marketed from Dec 8, 2022
0615-8371-140061583711414 TABLET in 1 BLISTER PACK (0615-8371-14)Marketed from Dec 8, 2022
0615-8371-280061583712828 TABLET in 1 BLISTER PACK (0615-8371-28)Marketed from Mar 29, 2024
0615-8371-390061583713930 TABLET in 1 BLISTER PACK (0615-8371-39)Marketed from Feb 11, 2022

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 50 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 0615-8371_8d918eb1-4133-4745-9afe-392ca3a699f9SPL ID 8d918eb1-4133-4745-9afe-392ca3a699f9SPL set ID 310c4b81-d2cf-4014-873d-e71d036105deRxCUI 856364, 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

N400615837105 followed by a unit qualifier and the quantity

Package 00615-8371-05. 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/1TabletOralAvKARE42291-868
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralProficient Rx LP71205-568
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralREMEDYREPACK INC.70518-2929
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-525
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-529
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralUnit Dose Solutions, Inc.87441-081
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralNorthwind Health Company, LLC51655-366
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralTeva Pharmaceuticals USA, Inc.50111-560

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