NDC codes

FDA NDC Directory
Product NDC (as listed)0555-0711Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00555-0711Add 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
0555-0711-020055507110200555071102100 TABLET in 1 BOTTLE (0555-0711-02)Marketed from Dec 9, 2021

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 — 300 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Teva Pharmaceuticals USA, Inc.NDC labeler code 0555
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071196
Marketing start
Listing expires
Identifiers
Product ID 0555-0711_3902eb87-aa22-4775-b56a-7cb86c5f920eSPL ID 3902eb87-aa22-4775-b56a-7cb86c5f920eSPL set ID 9c4da6ad-d4d1-4e8c-918d-8ac48512a93fRxCUI 856369UNII 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

N400555071102 followed by a unit qualifier and the quantity

Package 00555-0711-02. 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)

About NDC 0555-0711

What is NDC 0555-0711?
0555-0711 is the product NDC for Trazodone Hydrochloride, Trazodone hydrochloride 300 mg/1 tablet, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Trazodone Hydrochloride.
What is the active ingredient?
Trazodone hydrochloride.
Who is the labeler?
Teva Pharmaceuticals USA, Inc., NDC labeler code 0555. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Trazodone Hydrochloride?
157 other product NDCs are listed under this name. See all Trazodone Hydrochloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Trazodone Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralAmerican Health Packaging60687-96560687-0965-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralREMEDYREPACK INC.70518-476070518-4760-0070518-4760-0270518-4760-03+1 more
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralNorthwind Health Company, LLC82868-11682868-0116-90
Trazodone HydrochlorideTrazodone hydrochloride 25 mg/1Tablet, Film coatedOralTRUPHARMA LLC52817-39552817-0395-10
Trazodone HydrochlorideTrazodone hydrochloride 75 mg/1Tablet, Film coatedOralTRUPHARMA LLC52817-39652817-0396-10
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralREMEDYREPACK INC.70518-473770518-4737-0070518-4737-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralAmerican Health Packaging60687-95460687-0954-01
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralUnit Dose Solutions, Inc.87441-08087441-0080-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralUnit Dose Solutions, Inc.87441-08187441-0081-01
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1Tablet, Film coatedOralCoupler LLC67046-168467046-1684-03

All 158 Trazodone Hydrochloride NDCs

Other NDCs under ANDA 071196

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

FDA NDC Directory listings under ANDA 071196
ProductStrengthForm · routeLabelerProduct NDC
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralApotex Corp60505-2654
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralApotex Corp60505-2655
Trazodone HydrochlorideTrazodone hydrochloride 300 mg/1TabletOralApotex Corp60505-2659
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralREMEDYREPACK INC.70518-3403
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-513

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