FDA.reportPublic FDA data

NDC 0008-837 - Effexor XR

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
0008-837
Manufacturer
Stat Rx USA
Effective date
2009-10-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Effexor XR - Stat Rx USAStat Rx USA2009-10-27HUMAN PRESCRIPTION DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
venlafaxine hydrochlorideACTIVE INGREDIENT7D7RX5A8MOEFFEXOR XR (VENLAFAXINE HYDROCHLORIDE ) CAPSULE, EXTENDED RELEASE EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE [STAT RX USA]2
VENLAFAXINEACTIVE MOIETYGRZ5RCB1QGEFFEXOR XR (VENLAFAXINE HYDROCHLORIDE ) CAPSULE, EXTENDED RELEASE EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE [STAT RX USA]2

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 10 of 10 · 183 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
venlafaxineVENLAFAXINEProficient Rx LPcc3a1258-aafb-48cf-86f7-fcf59e0c6cdd2020-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
venlafaxine hydrochlorideVENLAFAXINE HYDROCHLORIDEDr.Reddy's Laboratories Ltd.7027be98-61d6-a986-c9df-60ceef5f7ff02018-12-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 313585
rxcui: 313583
rxcui: 313581
unii: 7D7RX5A8MO
81933ecb-2fd6-46a3-bf39-6516701756f9f2f03495-12b6-457a-901f-958b9c844bfd2009-10-27Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: 81933ecb-2fd6-46a3-bf39-6516701756f9
spl set id: f2f03495-12b6-457a-901f-958b9c844bfd

Reported adverse events (FAERS/openFDA)#

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