NDC codes

FDA NDC Directory
Product NDC (as listed)68071-2811Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-2811Add 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
68071-2811-36807128110330 TABLET in 1 BOTTLE (68071-2811-3)Marketed from Aug 26, 2026
68071-2811-56807128110525 TABLET in 1 BOTTLE (68071-2811-5)Marketed from Aug 10, 2022
68071-2811-66807128110660 TABLET in 1 BOTTLE (68071-2811-6)Marketed from Aug 10, 2022
68071-2811-86807128110815 TABLET in 1 BOTTLE (68071-2811-8)Marketed from Aug 10, 2022

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)
Acyclovir
Generic name (nonproprietary)
acyclovir
Active ingredients
Acyclovir — 400 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209366
Marketing start
Listing expires
Other FDA classes
DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
Identifiers
Product ID 68071-2811_59fbd4a5-9c28-c72f-e063-6394a90aeba8SPL ID 59fbd4a5-9c28-c72f-e063-6394a90aeba8SPL set ID e5e99a6b-79a6-7fdb-e053-2a95a90a8563RxCUI 197311UNII X4HES1O11FUPC 0368071281187
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

N468071281103 followed by a unit qualifier and the quantity

Package 68071-2811-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 209366

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

FDA NDC Directory listings under ANDA 209366
ProductStrengthForm · routeLabelerProduct NDC
AcyclovirAcyclovir 800 mg/1TabletOralBryant Ranch Prepack71335-2555
AcyclovirAcyclovir 800 mg/1TabletOralSQUARE PHARMACEUTICALS LIMITED76483-042
AcyclovirAcyclovir 400 mg/1TabletOralREMEDYREPACK INC.70518-4414
AcyclovirAcyclovir 400 mg/1TabletOralSQUARE PHARMACEUTICALS LIMITED76483-047
AcyclovirAcyclovir 400 mg/1TabletOralBionpharma Inc.69452-290
AcyclovirAcyclovir 800 mg/1TabletOralBionpharma Inc.69452-291
AcyclovirAcyclovir 400 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3573
AcyclovirAcyclovir 800 mg/1TabletOralREMEDYREPACK INC.70518-4450
AcyclovirAcyclovir 400 mg/1TabletOralBryant Ranch Prepack71335-2619
AcyclovirAcyclovir 400 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8203
AcyclovirAcyclovir 800 mg/1TabletOralA-S Medication Solutions50090-6335
AcyclovirAcyclovir 400 mg/1TabletOralDirect_Rx72189-631
AcyclovirAcyclovir 400 mg/1TabletOralBryant Ranch Prepack71335-9620

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