Acyclovir

Product NDC: 70518-2455
Requested package NDC: 70518-2455-0
11-digit product format: 705182455
Labeler code: 70518
Product ID: 70518-2455_4a291680-febd-5eac-e063-6394a90ab919
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: REMEDYREPACK INC.
Application: ANDA203834
Marketing category: ANDA
Marketing start: 2019-11-25
Substance: ACYCLOVIR
Active strength: 400 mg/1
Pharmacologic classes: DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	70518-2455	70518-2455-0	D	Discontinued by firm		2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A203834-001	ACYCLOVIR	ACYCLOVIR	400MG	TABLET / ORAL	AB		2013-10-29
A203834-002	ACYCLOVIR	ACYCLOVIR	800MG	TABLET / ORAL	AB	RS	2013-10-29

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 2 matching rows.

Application-product, TE code table
Application-product	TE code
A203834-001	AB
A203834-002	AB

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	RLD / RS	Approval date	Source SHA-256
2026-08-01 22:54:32	2026-06	A203834-001	ACYCLOVIR	400MG	TABLET / ORAL	AB		2013-10-29	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A203834-002	ACYCLOVIR	800MG	TABLET / ORAL	AB	RS	2013-10-29	`a50c72e98297…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-08-01 22:54:32	2026-06	A203834-001	AB	1	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A203834-002	AB	1	`a50c72e98297…`

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 2 · 22 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acyclovir	ACYCLOVIR	REMEDYREPACK INC.	6d0e492e-5359-49e8-812d-8c8e2e5d42f8	2026-07-24	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834 ndc (package): 70518-2455-0 ndc (product): 70518-2455 ndc11 (package): 70518245500
Acyclovir	ACYCLOVIR	REMEDYREPACK INC.	736679be-469e-4bdb-8e15-b10751c3dd60	2026-07-24	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	REMEDYREPACK INC.	38547daa-7d2f-4a7b-84d3-6e164984f958	2026-07-17	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	St. Mary's Medical Park Pharmacy	1493e22d-455d-b613-e063-6294a90afede	2026-06-04	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Bryant Ranch Prepack	dbdb7903-0991-413d-b1ad-ab0f1ae2d8f4	2026-06-04	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	PD-Rx Pharmaceuticals, Inc.	db0a0ce5-dc39-4bd3-8b97-21ce9c9999f0	2026-05-27	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Bryant Ranch Prepack	0e78d5e8-ae2d-4e84-b8c2-6765b1299c12	2026-05-21	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	PD-Rx Pharmaceuticals, Inc.	e8a0f9f8-294f-4dd6-bd55-10a6253f1aa8	2026-04-29	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Major Pharmaceuticals	46150f19-ce5d-42a0-80a7-f96fda2b9879	2026-02-18	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Preferred Pharmaceuticals, Inc.	b6d69697-12bb-4548-a6c3-2463cbf54f8f	2026-02-11	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Camber Pharmaceuticals, Inc.	0910335b-6796-459f-b97e-d7ef5439a060	2026-02-02	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Northwind Health Company, LLC	5dcfd21c-43f0-469c-be70-a4e74e6ccf88	2026-01-01	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Northwind Health Company, LLC	f6f56143-ea74-af87-e053-6394a90ae346	2026-01-01	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	Advanced Rx Pharmacy of Tennessee, LLC	f4c5779d-e4bf-4f2b-e053-2995a90a9187	2024-12-31	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	NuCare Pharmaceuticals,Inc.	638803d2-a172-486d-e053-2991aa0ab074	2024-07-16	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	NuCare Pharmaceuticals, Inc.	5176c7f9-9076-4797-e054-00144ff8d46c	2024-07-08	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	NuCare Pharmaceuticals,Inc.	83e82707-85b6-2fea-e053-2991aa0a99ef	2024-06-14	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	A-S Medication Solutions	e4f91376-9e18-41a4-aa5e-adcea0c625d9	2023-12-05	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	PharmPak, Inc.	d824fc07-9f03-4cb2-9bf8-ff7cc2955255	2022-10-09	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834
Acyclovir	ACYCLOVIR	PharmPak, Inc.	8fb01f23-e2bd-6850-e053-2995a90a7cc5	2022-10-09	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 203834 application number: ANDA203834

Additional Listing Data#

Finished product: Yes
Brand name base: Acyclovir
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACYCLOVIR	400 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
X4HES1O11F	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
197311	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
6d0e492e-5359-49e8-812d-8c8e2e5d42f8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
33190c02-82e1-0a4d-d716-9ccd23588463	Product name	5	20250225
c367d1da-5a72-8966-6d11-1eb9a73ae758	Product name	3	20231115
5518bf13-db2f-2e9c-3679-e70ecf03752c	Product name	9	20210614
27897900-0e40-497b-97e1-88057e68fe6c	Product name	4	20200710
ca834e59-e669-229c-9288-0ccb76dc373e	Product name	9	20200220
d7f95c49-d3e1-4bbc-a389-e9cd73f59a28	Product name	1	20190702
fb15b394-3715-4c87-a447-421489aa8739	Product name	3	20170727
7bdc4804-3832-c0df-e519-72b6d47c9792	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70518-2455-0	Acyclovir	30 in 1 BLISTER PACK	TABLET	30	15
70518-2455-1	Acyclovir	15 in 1 BOTTLE, PLASTIC	TABLET	15	15
70518-2455-2	Acyclovir	30 in 1 BOTTLE, PLASTIC	TABLET	30	15
70518-2455-3	Acyclovir	21 in 1 BOTTLE, PLASTIC	TABLET	21	15
70518-2455-4	Acyclovir	50 in 1 BOTTLE, PLASTIC	TABLET	50	15

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70518-2455-1	EA - Each	70518-2455	29b478eb-6a37-414a-a3da-4aa3708ef4f5	1	2023-01-09
70518-2455-2	EA - Each	70518-2455	888ff41b-37dc-45c7-9ed0-0fbe6b6be70b	1	2026-01-08
70518-2455-3	EA - Each	70518-2455	c17c0354-d3fa-49ae-aac7-3135cd67e3ae	1	2023-01-09

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-2455	ACYCLOVIR TABLET [REMEDYREPACK INC.]	13	Current NDC, Legacy NDC, 5 package rows	20250316_6d0e492e-5359-49e8-812d-8c8e2e5d42f8.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
X4HES1O11F	ACYCLOVIR	59277-89-3	ACYCLOVIR

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
197311	acyclovir 400 MG Oral Tablet	PSN	6d0e492e-5359-49e8-812d-8c8e2e5d42f8	15
197311	acyclovir 400 MG Oral Tablet	SCD	6d0e492e-5359-49e8-812d-8c8e2e5d42f8	15
197311	acycycloguanosine 400 MG Oral Tablet	SY	6d0e492e-5359-49e8-812d-8c8e2e5d42f8	15

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70518-2455-0	70518245500	30 TABLET in 1 BLISTER PACK (70518-2455-0)	30 tablet	2019-11-25	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
PRESCRIBING INFORMATION Acyclovir Tablets, USP Rx only	REMEDYREPACK INC.	2026-07-24	HUMAN PRESCRIPTION DRUG LABEL	16