NDC 62157-895 - Cidofovir Dihydrate

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: 62157-895
Package NDCs from labels: 62157-895-01
Manufacturer: AX Pharmaceutical Corp
Effective date: 2019-07-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Cidofovir Dihydrate - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2019-07-22	BULK INGREDIENT

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 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CIDOFOVIR DIHYDRATE	CIDOFOVIR DIHYDRATE	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	44966a7e-d777-40fb-956f-d0f31f737848	2023-10-25	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JIL713Q00N
CIDOFOVIR	CIDOFOVIR ANHYDROUS	Mylan Institutional LLC	56541229-8c1a-4550-8951-2415ed08e7e9	2021-04-15	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JIL713Q00N

Reported adverse events (FAERS/openFDA)#

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