NDC 86032-021 - 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
86032-021
Package NDCs from labels
86032-021-01
Manufacturer
Evereen Shanghai Biotechnology Ltd.
Effective date
2023-02-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AcyclovirEvereen Shanghai Biotechnology Ltd.2023-02-08BULK INGREDIENT - ANIMAL DRUG

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 9 of 9 · 167 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcyclovirACYCLOVIRACTAVIS PHARMA, INC.b360a808-a24d-4f3c-89a7-9941422d17d62020-10-31Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
ZoviraxACYCLOVIRBausch Health US, LLC50278e0e-da1e-45ee-9fcb-672b2a2199112020-10-31Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
acyclovirACYCLOVIRAsclemed USA, Inc.e186fdc9-b60e-4280-8d60-36cae9f2838f2020-09-25Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
XereseACYCLOVIR AND HYDROCORTISONEBausch Health US LLC3b6ac164-0f1e-4f36-94a1-1fdb07d710f52020-08-03Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
acyclovirACYCLOVIRProficient Rx LP51052f0e-1a07-405a-a962-981ce9439e022020-02-01Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
AcyclovirACYCLOVIRXiromed, LLC3e222423-3bf2-6584-6d54-447b1b26dc422020-01-30Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F
AcyclovirACYCLOVIRProficient Rx LP6714cfd9-97d3-4290-b618-54594d89cf4e2020-01-01Warnings, Adverse reactionsExact identifier
unii: X4HES1O11F

Reported adverse events (FAERS/openFDA)#

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