NDC 82922-027 - Truemed Group LLC

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
82922-027
Package NDCs from labels
82922-027-01
Manufacturer
Truemed Group LLC
Effective date
2022-08-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
RISPERIDONE - Truemed Group LLCTruemed Group LLC2022-08-10HUMAN PRESCRIPTION DRUG LABEL

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 4 of 4 · 66 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RISPERIDONERISPERIDONEProficient Rx LP1b5c9889-4dc3-48df-8629-4ac099e2b4c02022-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L6UH7ZF8HC
RisperidoneRISPERIDONESun Pharmaceutical Industries, Inc.f91f551e-926f-440d-83d2-357e9d7484fe2022-07-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L6UH7ZF8HC
RISPERIDONERISPERIDONEProficient Rx LP394c7e27-52a2-4d4c-8c6e-fe37b03266ae2022-06-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L6UH7ZF8HC
risperidoneRISPERIDONEProficient Rx LPb611fe52-1787-47e6-8a6b-1999a4e4f22c2021-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L6UH7ZF8HC
RISPERIDONERISPERIDONEAphena Pharma Solutions - Tennessee, LLCac152803-d75f-4c3c-bc49-8663b21a3a822019-04-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L6UH7ZF8HC
RisperidoneRISPERIDONEAphena Pharma Solutions - Tennessee, LLC58e422ec-da66-41b0-83c1-aefd940beda02019-04-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L6UH7ZF8HC

Reported adverse events (FAERS/openFDA)#

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