What is NDC 70518-4661?

70518-4661 is the product NDC for Valacyclovir, Valacyclovir hydrochloride 500 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

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 Valacyclovir?

51 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Valacyclovir NDC 70518-4661 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4661Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4661Add 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 NDC	11-digit (billing)	Package	Copy
70518-4661-0	70518466100	30 TABLET in 1 BOTTLE, PLASTIC (70518-4661-0)Marketed from May 14, 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): Valacyclovir
Generic name (nonproprietary): valacyclovir
Active ingredients: Valacyclovir hydrochloride — 500 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 209553
Marketing start: May 14, 2026
Listing expires: Dec 31, 2027
Other FDA classes: DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
Identifiers: Product ID 70518-4661_52184b4f-f400-eeb8-e063-6294a90ab18fSPL ID 52184b4f-f400-eeb8-e063-6294a90ab18fSPL set ID 6ff2068f-1002-4d84-bd65-081d5b4082b1RxCUI 313565UNII G447S0T1VC
Pharmacologic class: Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase 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

N470518466100 followed by a unit qualifier and the quantity

Package 70518-4661-00. 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 May 18, 2026.

Indications (excerpt from the label)

Valacyclovir tablets are a deoxynucleoside analogue DNA polymerase inhibitor indicated for: Adult Patients ( 1.1 ) Cold Sores (Herpes Labialis) Genital Herpes Treatment in immunocompetent patients (initial or recurrent episode) Suppression in immunocompetent or HIV-1-infected patients Reduction of transmission Herpes Zoster Pediatric Patients ( 1.2 ) Cold Sores (Herpes Labialis) Chickenpox Limitations of Use ( 1.3 ) The efficacy and safety of valacyclovir tablets have not been established in immunocompromised patients other than for the suppression of genital herpes in HIV-1-infected patients. 1.1 Adult Patients Cold Sores (Herpes Labialis) Valacyclovir tablets are indicated for treatment of…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4661

What is NDC 70518-4661?: 70518-4661 is the product NDC for Valacyclovir, Valacyclovir hydrochloride 500 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Valacyclovir.
What is the active ingredient?: Valacyclovir 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 Valacyclovir?: 51 other product NDCs are listed under this name. See all Valacyclovir 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 Valacyclovir NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-856	60760-0856-42
Valacyclovir	Valacyclovir hydrochloride 1 g/1	Tablet, Film coatedOral	Coupler LLC	67046-1347	67046-1347-03
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1071	67046-1071-03
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4105	68788-4105-0368788-4105-09
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4417	70518-4417-00
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Direct_Rx	72189-630	72189-0630-2072189-0630-30
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	Direct _Rx	72189-594	72189-0594-0472189-0594-1672189-0594-21+1 more
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8705	68788-8705-0068788-8705-0168788-8705-02+4 more
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	REMEDYREPACK INC.	70518-4100	70518-4100-0070518-4100-0170518-4100-02+5 more
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	A-S Medication Solutions	50090-6581	50090-6581-0050090-6581-0150090-6581-02+1 more

All 52 Valacyclovir NDCs

Other NDCs under ANDA 209553

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

FDA NDC Directory listings under ANDA 209553
Product	Strength	Form · route	Labeler	Product NDC
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	A-S Medication Solutions	50090-6581
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	A-S Medication Solutions	50090-7270
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	A-S Medication Solutions	50090-7484
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-856
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Chartwell RX, LLC	62135-613
Valacyclovir	Valacyclovir hydrochloride 1 g/1	TabletOral	Chartwell RX, LLC	62135-614
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	Redpharm Drug	67296-2146
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3624
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4105
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8705
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Yiling Pharmaceutical, Inc.	69117-0010
Valacyclovirvalacyclovir hydrochloride	Valacyclovir hydrochloride 1 g/1	TabletOral	Yiling Pharmaceutical, Inc.	69117-0011
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-262
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-263
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	REMEDYREPACK INC.	70518-4100
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	Bryant Ranch Prepack	71335-2534
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-2566
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	Direct _Rx	72189-594
Valacyclovir	Valacyclovir hydrochloride 500 mg/1	TabletOral	Direct_Rx	72189-630
Valacyclovir	Valacyclovir hydrochloride 1000 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-586

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