NDC 68094-019-59 - Guanfacine

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
68094-019
Requested NDC
68094-019-59
Package NDCs from labels
68094-019-59, 68094-019-62
Manufacturer
Precision Dose, Inc.
Effective date
2019-08-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Guanfacine Tablets, USPPrecision Dose, Inc.2019-08-08HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68094-019-59EA - Each68094-01962174b6a-15ef-4188-8320-777e66e35b8212019-09-05
68094-019-62EA - Each68094-01985084b03-e2f9-44c9-bb51-ffee0ba6e68b12019-09-05

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 4 of 4 · 65 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Guanfacine extended-releaseGUANFACINEA-S Medication Solutions07797c4a-a799-436b-a77c-a2861a811a992023-05-23Warnings, Adverse reactionsExact identifier
unii: PML56A160O
eb56056a-3ba0-4f92-8d62-01e0f6a2392385567945-ff78-4deb-a033-167230ba43032022-10-17Adverse reactionsExact identifier
spl set id: 85567945-ff78-4deb-a033-167230ba4303
Guanfacine HydrochlorideGUANFACINE HYDROCHLORIDEUnichem Pharmaceuticals (USA), Inc.14146031-8d56-469b-8de8-fe3cf1712e782021-03-30Adverse reactionsExact identifier
rxcui: 197746
rxcui: 197745
GuanfacineGUANFACINEProficient Rx LP09442806-db7b-49de-8ffc-e4cb831383492020-07-01Adverse reactionsExact identifier
rxcui: 197745
unii: PML56A160O
guanfacineGUANFACINEActavis Pharma, Inc.3a171942-37af-430d-8b9d-bb678ca2be4b2020-01-31Warnings, Adverse reactionsExact identifier
unii: PML56A160O

Reported adverse events (FAERS/openFDA)#

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