NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0470Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0470Add 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
71335-0470-07133504700090 CAPSULE in 1 BOTTLE (71335-0470-0)Marketed from Jul 9, 2024
71335-0470-17133504700130 CAPSULE in 1 BOTTLE (71335-0470-1)Marketed from Jul 11, 2019
71335-0470-27133504700225 CAPSULE in 1 BOTTLE (71335-0470-2)Marketed from Mar 28, 2018
71335-0470-37133504700335 CAPSULE in 1 BOTTLE (71335-0470-3)Marketed from Jun 22, 2018
71335-0470-47133504700450 CAPSULE in 1 BOTTLE (71335-0470-4)Marketed from Jul 9, 2024
71335-0470-571335047005100 CAPSULE in 1 BOTTLE (71335-0470-5)Marketed from Jul 9, 2024
71335-0470-67133504700640 CAPSULE in 1 BOTTLE (71335-0470-6)Marketed from Jul 9, 2024
71335-0470-77133504700760 CAPSULE in 1 BOTTLE (71335-0470-7)Marketed from Jan 4, 2019
71335-0470-871335047008120 CAPSULE in 1 BOTTLE (71335-0470-8)Marketed from Jul 9, 2024
71335-0470-97133504700920 CAPSULE in 1 BOTTLE (71335-0470-9)Marketed from Jul 9, 2024

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 — 200 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075677
Marketing start
Marketing end
Other FDA classes
DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
Identifiers
Product ID 71335-0470_1848497f-16ba-4911-b27f-a4b5e645767fSPL ID 1848497f-16ba-4911-b27f-a4b5e645767fSPL set ID 2b600b5d-ce91-461f-b9d1-75b969daf8e9RxCUI 197310UNII X4HES1O11F
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

N471335047000 followed by a unit qualifier and the quantity

Package 71335-0470-00. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Herpes Zoster Infections Acyclovir capsule is indicated for the acute treatment of herpes zoster (shingles). Genital Herpes Acyclovir capsule is indicated for the treatment of initial episodes and the management of recurrent episodes of genital herpes. Chickenpox Acyclovir capsule is indicated for the treatment of chickenpox (varicella).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0470

What is NDC 71335-0470?
71335-0470 is the product NDC for Acyclovir, Acyclovir 200 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Acyclovir.
What is the active ingredient?
Acyclovir.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Acyclovir?
192 other product NDCs are listed under this name. See all Acyclovir 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 Acyclovir NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
acyclovirAcyclovir 50 mg/gOintmentTopicalc68788-414268788-4142-01
AcyclovirAcyclovir 200 mg/1CapsuleOralCardinal Health 107, LLC55154-019955154-0199-00
acyclovirAcyclovir 800 mg/1TabletOralNorthwind Health Company, LLC82868-10782868-0107-3082868-0107-35
AcyclovirAcyclovir 50 mg/gOintmentTopicalAryeh Pharma Corp85957-03685957-0036-0185957-0036-0285957-0036-03
AcyclovirAcyclovir 200 mg/1CapsuleOralAvet Pharmaceuticals Inc.23155-96223155-0962-0123155-0962-05
AcyclovirAcyclovir 200 mg/1CapsuleOralFlorida Pharmaceutical Products, LLC71921-14671921-0146-01
AcyclovirAcyclovir 200 mg/1CapsuleOralMajor Pharmaceuticals0904-751900904-7519-61
AcyclovirAcyclovir 400 mg/1TabletOralAurobindo Pharma Limited59651-96559651-0965-0159651-0965-0559651-0965-10
AcyclovirAcyclovir 800 mg/1TabletOralAurobindo Pharma Limited59651-96659651-0966-0159651-0966-0559651-0966-10
AcyclovirAcyclovir 800 mg/1TabletOralREMEDYREPACK INC.70518-445070518-4450-0070518-4450-01

All 193 Acyclovir NDCs

Other NDCs under ANDA 075677

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

FDA NDC Directory listings under ANDA 075677
ProductStrengthForm · routeLabelerProduct NDC
AcyclovirAcyclovir 200 mg/1CapsuleOralApotex Corp.60505-0042
AcyclovirAcyclovir 200 mg/1CapsuleOralProficient Rx LP71205-243
AcyclovirAcyclovir 200 mg/1CapsuleOralBryant Ranch Prepack72162-1704

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