NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4737Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4737Add 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
70518-4737-0705184737007051847370090 TABLET in 1 BOTTLE, PLASTIC (70518-4737-0)Marketed from Aug 26, 2026
70518-4737-1705184737017051847370130 TABLET in 1 BLISTER PACK (70518-4737-1)Marketed from Aug 27, 2026

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 — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218988
Marketing start
Listing expires
Identifiers
Product ID 70518-4737_5a068dad-0446-1236-e063-6394a90aa6afSPL ID 5a068dad-0446-1236-e063-6394a90aa6afSPL set ID 3b2e61b0-414c-48ae-9e13-06470c302c67RxCUI 856373UNII 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

N470518473700 followed by a unit qualifier and the quantity

Package 70518-4737-00. 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 70518-4737

What is NDC 70518-4737?
70518-4737 is the product NDC for Trazodone Hydrochloride, Trazodone hydrochloride 100 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, 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?
REMEDYREPACK INC., NDC labeler code 70518. 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 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
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralREMEDYREPACK INC.70518-469070518-4690-00

All 158 Trazodone Hydrochloride NDCs

Other NDCs under ANDA 218988

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

FDA NDC Directory listings under ANDA 218988
ProductStrengthForm · routeLabelerProduct NDC
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralGolden State Medical Supply, Inc.51407-946
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralGolden State Medical Supply, Inc.51407-947
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralCoupler LLC67046-1506
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralCoupler LLC67046-1540
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralGranules Pharmaceuticals Inc.70010-231
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralGranules Pharmaceuticals Inc.70010-232
Trazodone HydrochlorideTrazodone hydrochloride 150 mg/1TabletOralGranules Pharmaceuticals Inc.70010-233
Trazodone HydrochlorideTrazodone hydrochloride 300 mg/1TabletOralGranules Pharmaceuticals Inc.70010-234
Trazodone HydrochlorideTrazodone hydrochloride 50 mg/1TabletOralREMEDYREPACK INC.70518-4760
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralNorthwind Health Company, LLC82868-116
Trazodone HydrochlorideTrazodone hydrochloride 100 mg/1TabletOralUnit Dose Solutions, Inc.87441-080

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