FDA.reportPublic FDA data

NDC 69117-0018-01 - Acyclovir

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
69117-0018
Requested NDC
69117-0018-01
Package NDCs from labels
69117-0018-1, 69117-0018-2, 69117-0018-01
Manufacturer
YILING PHARMACEUTICAL, INC. | YILING PHARMACEUTICAL LTD
Effective date
2025-12-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Acyclovir - YILING PHARMACEUTICAL, INC. | YILING PHARMACEUTICAL LTDYILING PHARMACEUTICAL, INC. | YILING PHARMACEUTICAL LTD2025-12-30HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - Proficient Rx LPProficient Rx LP2024-10-01HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - RPK Pharmaceuticals, Inc.RPK Pharmaceuticals, Inc.2022-03-30HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - Bryant Ranch PrepackBryant Ranch Prepack2022-02-14HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - Bryant Ranch PrepackBryant Ranch Prepack2022-02-14HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - Bryant Ranch PrepackBryant Ranch Prepack2022-02-14HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - REMEDYREPACK INC.REMEDYREPACK INC.2021-06-22HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - Preferred Pharmaceuticals Inc.Preferred Pharmaceuticals Inc.2021-02-19HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2021-02-19HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - Denton Pharma, Inc. DBA Northwind PharmaceuticalsDenton Pharma, Inc. DBA Northwind Pharmaceuticals2020-09-14HUMAN PRESCRIPTION DRUG LABEL
Acyclovir - REMEDYREPACK INC.REMEDYREPACK INC.2019-09-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69117-0018-1Acyclovir100 in 1 BOTTLETABLET1009
69117-0018-2Acyclovir500 in 1 BOTTLETABLET5009

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69117-0018ACYCLOVIR TABLET [YILING PHARMACEUTICAL, INC.]8Current NDC, Legacy NDC, 2 package rows20250101_677edfd5-2d04-b932-e053-2a91aa0a26b0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69117-0018-1EA - Each69117-00186e50aa43-459d-4c85-b38b-71f8aadadd3612018-09-05
69117-0018-2EA - Each69117-0018a8aa51bf-b186-4f0d-833f-47393834f59612018-09-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 9 · 178 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ACYCLOVIRACYCLOVIRREMEDYREPACK INC.c1744e01-0e40-4851-8ffc-c3bf29dd7c2b2026-08-31Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
AcyclovirACYCLOVIRNuCare Pharmaceuticals, Inc.5176c7f9-9076-4797-e054-00144ff8d46c2026-08-27Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
AcyclovirACYCLOVIRNuCare Pharmaceuticals,Inc.e5e99a6b-79a6-7fdb-e053-2a95a90a85632026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 197311
unii: X4HES1O11F
AcyclovirACYCLOVIRPD-Rx Pharmaceuticals, Inc.58dc1402-6098-9cb3-e063-6294a90a062b2026-08-19Warnings, Adverse reactionsExact identifier
application number: ANDA210401
rxcui: 197311
unii: X4HES1O11F
acyclovirACYCLOVIRNorthwind Health Company, LLC50c58161-3944-7367-e063-6394a90a62862026-08-19Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
ACYCLOVIRACYCLOVIRCardinal Health 107, LLC4cc7d67f-35fa-4238-a581-4810645083cf2026-08-13Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
acyclovirACYCLOVIRc59007780-d736-4195-a204-7f85a709ed462026-08-12Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
ACYCLOVIRACYCLOVIRHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.0de2f5c7-9e75-4bdf-9c28-e026cc6694b42026-07-24Warnings, Adverse reactionsExact identifier
rxcui: 197311
unii: X4HES1O11F
acyclovirACYCLOVIRPD-Rx Pharmaceuticals, Inc.86c43bdf-c5bf-47cd-8dfd-8112638258782026-07-24Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
AcyclovirACYCLOVIRREMEDYREPACK INC.6d0e492e-5359-49e8-812d-8c8e2e5d42f82026-07-24Warnings, Adverse reactionsExact identifier
rxcui: 197311
unii: X4HES1O11F
AcyclovirACYCLOVIRREMEDYREPACK INC.736679be-469e-4bdb-8e15-b10751c3dd602026-07-24Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
AcyclovirACYCLOVIRREMEDYREPACK INC.38547daa-7d2f-4a7b-84d3-6e164984f9582026-07-17Warnings, Adverse reactionsExact identifier
rxcui: 197311
unii: X4HES1O11F
ACYCLOVIRACYCLOVIRMajor Pharmaceuticals9b254eed-8ea1-469b-bf27-f5670cd99e8d2026-07-14Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
AcyclovirACYCLOVIRATLANTIC BIOLOGICALS CORP.da5a809c-6ddc-4609-9a34-ccb3d2d439762026-07-10Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
ACYCLOVIRACYCLOVIRHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.85332671-0e3a-4445-a337-e1266886b9cf2026-07-08Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
ACYCLOVIRACYCLOVIRAmerican Health Packaging05f42300-2a06-45f1-a9b9-6e5c84ae58ec2026-07-01Warnings, Adverse reactionsExact identifier
rxcui: 197311
unii: X4HES1O11F
acyclovirACYCLOVIRREMEDYREPACK INC.499c6a98-0614-4ded-8526-909942bae8a42026-06-26Warnings, Adverse reactionsExact identifier
rxcui: 197311
unii: X4HES1O11F
AcyclovirACYCLOVIRREMEDYREPACK INC.37a51d9c-1f39-4065-8c7d-6528ac6de91c2026-06-23Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
ACYCLOVIRACYCLOVIRAlembic Pharmaceuticals Inc.878615c2-09ea-44ce-8c30-7a7f16acb20c2026-06-18Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
acyclovirACYCLOVIRBryant Ranch Prepackdb35fce0-d7a3-4589-ba60-d78cdb1119cb2026-06-18Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.