What is NDC 71335-2261?

71335-2261 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.

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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

acyclovir NDC 71335-2261 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2261Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2261Add 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
71335-2261-0	71335226100	90 CAPSULE in 1 BOTTLE (71335-2261-0)Marketed from Oct 27, 2023
71335-2261-1	71335226101	30 CAPSULE in 1 BOTTLE (71335-2261-1)Marketed from Oct 27, 2023
71335-2261-2	71335226102	25 CAPSULE in 1 BOTTLE (71335-2261-2)Marketed from Oct 27, 2023
71335-2261-3	71335226103	35 CAPSULE in 1 BOTTLE (71335-2261-3)Marketed from Oct 27, 2023
71335-2261-4	71335226104	50 CAPSULE in 1 BOTTLE (71335-2261-4)Marketed from Oct 27, 2023
71335-2261-5	71335226105	100 CAPSULE in 1 BOTTLE (71335-2261-5)Marketed from Oct 27, 2023
71335-2261-6	71335226106	40 CAPSULE in 1 BOTTLE (71335-2261-6)Marketed from Oct 27, 2023
71335-2261-7	71335226107	60 CAPSULE in 1 BOTTLE (71335-2261-7)Marketed from Oct 27, 2023
71335-2261-8	71335226108	120 CAPSULE in 1 BOTTLE (71335-2261-8)Marketed from Oct 27, 2023
71335-2261-9	71335226109	20 CAPSULE in 1 BOTTLE (71335-2261-9)Marketed from Oct 27, 2023

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 204313
Marketing start: Aug 23, 2019
Listing expires: Dec 31, 2026
Other FDA classes: DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
Identifiers: Product ID 71335-2261_1bed7dd6-b341-487f-8cdb-45c1d7906e32SPL ID 1bed7dd6-b341-487f-8cdb-45c1d7906e32SPL set ID c818e86c-a4d0-48cd-a888-fa1ee9e2aa19RxCUI 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

N471335226100 followed by a unit qualifier and the quantity

Package 71335-2261-00. 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 Sep 22, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Herpes Zoster Infections: Acyclovir capsules are indicated for the acute treatment of herpes zoster (shingles). Genital Herpes: Acyclovir capsules are indicated for the treatment of initial episodes and the management of recurrent episodes of genital herpes. Chickenpox: Acyclovir capsules are 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 71335-2261

What is NDC 71335-2261?: 71335-2261 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
acyclovir	Acyclovir 50 mg/g	OintmentTopical	c	68788-4142	68788-4142-01
Acyclovir	Acyclovir 200 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0199	55154-0199-00
acyclovir	Acyclovir 800 mg/1	TabletOral	Northwind Health Company, LLC	82868-107	82868-0107-3082868-0107-35
Acyclovir	Acyclovir 50 mg/g	OintmentTopical	Aryeh Pharma Corp	85957-036	85957-0036-0185957-0036-0285957-0036-03
Acyclovir	Acyclovir 200 mg/1	CapsuleOral	Avet Pharmaceuticals Inc.	23155-962	23155-0962-0123155-0962-05
Acyclovir	Acyclovir 200 mg/1	CapsuleOral	Florida Pharmaceutical Products, LLC	71921-146	71921-0146-01
Acyclovir	Acyclovir 200 mg/1	CapsuleOral	Major Pharmaceuticals	0904-7519	00904-7519-61
Acyclovir	Acyclovir 400 mg/1	TabletOral	Aurobindo Pharma Limited	59651-965	59651-0965-0159651-0965-0559651-0965-10
Acyclovir	Acyclovir 800 mg/1	TabletOral	Aurobindo Pharma Limited	59651-966	59651-0966-0159651-0966-0559651-0966-10
Acyclovir	Acyclovir 800 mg/1	TabletOral	REMEDYREPACK INC.	70518-4450	70518-4450-0070518-4450-01

All 193 acyclovir NDCs

Other NDCs under ANDA 204313

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

FDA NDC Directory listings under ANDA 204313
Product	Strength	Form · route	Labeler	Product NDC
acyclovir	Acyclovir 200 mg/1	CapsuleOral	A-S Medication Solutions	50090-7216
acyclovir	Acyclovir 200 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-965
acyclovir	Acyclovir 200 mg/1	CapsuleOral	Zydus Lifesciences Limited	65841-829
Acyclovir	Acyclovir 200 mg/1	CapsuleOral	NuCare Pharmaceuticals,Inc.	68071-2526
acyclovir	Acyclovir 200 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3436
acyclovir	Acyclovir 200 mg/1	CapsuleOral	Viona Pharmaceuticals Inc	72578-002
acyclovir	Acyclovir 200 mg/1	CapsuleOral	PD-Rx Pharmaceuticals, Inc.	72789-536
acyclovir	Acyclovir 200 mg/1	CapsuleOral	Proficient Rx LP	82804-245