NDC codes

FDA NDC Directory
Product NDC (as listed)63187-950Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0950Add 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
63187-950-04631870950044 TABLET, FILM COATED in 1 BOTTLE (63187-950-04)Marketed from Jan 1, 2018
63187-950-06631870950066 TABLET, FILM COATED in 1 BOTTLE (63187-950-06)Marketed from Jan 1, 2018
63187-950-106318709501010 TABLET, FILM COATED in 1 BOTTLE (63187-950-10)Marketed from Jul 25, 2023
63187-950-146318709501414 TABLET, FILM COATED in 1 BOTTLE (63187-950-14)Marketed from Jan 1, 2018
63187-950-206318709502020 TABLET, FILM COATED in 1 BOTTLE (63187-950-20)Marketed from Sep 25, 2023
63187-950-216318709502121 TABLET, FILM COATED in 1 BOTTLE (63187-950-21)Marketed from Jan 1, 2018
63187-950-306318709503030 TABLET, FILM COATED in 1 BOTTLE (63187-950-30)Marketed from Jan 1, 2018
63187-950-606318709506060 TABLET, FILM COATED in 1 BOTTLE (63187-950-60)Marketed from Jan 1, 2018
63187-950-906318709509090 TABLET, FILM COATED in 1 BOTTLE (63187-950-90)Marketed from Jan 1, 2018

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)
Valacyclovir
Generic name (nonproprietary)
valacyclovir
Active ingredients
Valacyclovir hydrochloride — 1 g/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203047
Marketing start
Listing expires
Other FDA classes
DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
Identifiers
Product ID 63187-950_441151ec-31f4-413c-8764-11fc16fb2adaSPL ID 441151ec-31f4-413c-8764-11fc16fb2adaSPL set ID 8794a786-245a-42a3-b33a-9b0ed1dd46acRxCUI 313564UNII G447S0T1VCUPC 0363187950101
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

N463187095004 followed by a unit qualifier and the quantity

Package 63187-0950-04. 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 .

Indications (excerpt from the label)

Valacyclovir tablet, USP is a nucleoside 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-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, USP have not been established in immunocompromised patients other than for the suppression of genital herpes in HIV-infected patients. 1.1 Adult patients Cold Sores (Herpes Labialis): Valacyclovir tablets, USP are indicated…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203047

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

FDA NDC Directory listings under ANDA 203047
ProductStrengthForm · routeLabelerProduct NDC
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralQuallent Pharmaceuticals Health LLC82009-041
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7702
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralProficient Rx LP82804-212
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2402
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-7587
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4805
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralBryant Ranch Prepack71335-0630
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3747
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3749
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3749
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-2510
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralCoupler LLC67046-1071
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralA-S Medication Solutions50090-2575
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-452
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-704
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-705
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralSt Mary's Medical Park Pharmacy60760-469
ValacyclovirValacyclovir hydrochloride 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4417
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralCoupler LLC67046-1347
ValacyclovirValacyclovir hydrochloride 1 g/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-771

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