FDA.reportPublic FDA data

NDC 80425-0313-01 - Fluoxetine

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
80425-0313
Requested NDC
80425-0313-01
Package NDCs from labels
80425-0313-1, 80425-0313-2, 80425-0313-3, 80425-0313-01
Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC
Effective date
2024-12-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Fluoxetine - Advanced Rx Pharmacy of Tennessee, LLCAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80425-0313-1Fluoxetine30 in 1 BOTTLECAPSULE302
80425-0313-2Fluoxetine60 in 1 BOTTLECAPSULE602
80425-0313-3Fluoxetine90 in 1 BOTTLECAPSULE902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80425-0313FLUOXETINE CAPSULE [ADVANCED RX PHARMACY OF TENNESSEE, LLC]2Current NDC, 3 package rows20250102_f917063a-226e-0978-e053-6294a90aeb4b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80425-0313-1EA - Each80425-0313b8d1d31a-fff6-4b9c-a9b3-e011b8c7eb4712023-06-06
80425-0313-2EA - Each80425-0313829bc627-e21e-4aa1-99b3-4b8ba39cdb6f12023-06-06
80425-0313-3EA - Each80425-0313562d5109-ba29-492b-84e6-90b21d9adfc712023-06-06

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 9 · 167 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FluoxetineFLUOXETINE HYDROCHLORIDEREMEDYREPACK INC.a08dadff-f209-48dc-b597-6f085be136402026-09-10Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA204597
rxcui: 310385
unii: I9W7N6B1KJ
FluoxetineFLUOXETINE HYDROCHLORIDEMajor Pharmaceuticals76b264ce-2a13-4511-8e21-4ffad0a327f92026-08-31Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 310384
rxcui: 310385
unii: I9W7N6B1KJ
FluoxetineFLUOXETINE HYDROCHLORIDEScieGen Pharmaceuticals, Inc.23899405-007b-48d9-82a9-a530b8e907842026-08-20Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA204597
ndc (product): 50228-114
rxcui: 313989
rxcui: 310384
rxcui: 310385
spl id: 16ff2e11-8dd1-4058-ace2-0fa2926997fb
spl set id: 23899405-007b-48d9-82a9-a530b8e90784
unii: I9W7N6B1KJ
FLUOXETINEFLUOXETINEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.6f4e4e9f-9ded-452f-b3ef-ab6aa9c729522026-08-11Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 313989
rxcui: 310384
rxcui: 310385
unii: I9W7N6B1KJ
FluoxetineFLUOXETINE HYDROCHLORIDEAphena Pharma Solutions - Tennessee, LLC583c5021-2948-7db4-e063-6294a90ae7dc2026-08-04Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA204597
rxcui: 310385
unii: I9W7N6B1KJ
FluoxetineFLUOXETINEREMEDYREPACK INC.24926986-7552-4f1a-8366-f035bbd071042026-07-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 310385
unii: I9W7N6B1KJ
fluoxetine hydrochlorideFLUOXETINE HYDROCHLORIDEBryant Ranch Prepackd4043133-38de-4faa-bb76-8fafa59138442026-07-16Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
fluoxetine hydrochlorideFLUOXETINE HYDROCHLORIDEBryant Ranch Prepacka04a5bed-d051-4bb4-ae20-b09b10d5c1812026-07-16Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
FluoxetineFLUOXETINE HYDROCHLORIDEAmerican Health Packaging7bee936b-0130-4a6b-a974-956aef5486d92026-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 313989
unii: I9W7N6B1KJ
FluoxetineFLUOXETINEAmerican Health Packaging9965a672-7842-4926-9063-b76317c748622026-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 313989
unii: I9W7N6B1KJ
FluoxetineFLUOXETINEAurobindo Pharma Limiteda9ed97dd-8041-4a02-889c-dcb8b2805f362026-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
FluoxetineFLUOXETINEAurobindo Pharma Limited09fb3100-1e06-4cdc-8016-7e4f5d0974902026-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
FLUOXETINE HYDROCHLORIDEFLUOXETINE HYDROCHLORIDESun Pharmaceutical Industries, Inc.77b6ae48-8e3a-42e6-9b5a-aeed750861e82026-07-14Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
fluoxetine hydrochlorideFLUOXETINE HYDROCHLORIDEBryant Ranch Prepackfb0608d9-1ae3-43be-8a20-e9f34e9558622026-07-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
fluoxetine hydrochlorideFLUOXETINE HYDROCHLORIDEBryant Ranch Prepackd5a267cb-08bd-4530-a7a8-2bceddd828e52026-07-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
fluoxetine hydrochlorideFLUOXETINE HYDROCHLORIDEBryant Ranch Prepack72e391aa-1a46-4589-8550-f83ac9241cf12026-07-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
FluoxetineFLUOXETINE HYDROCHLORIDEREMEDYREPACK INC.32afb28a-dc4c-4a7e-9701-1825f805e7df2026-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 310384
unii: I9W7N6B1KJ
FluoxetineFLUOXETINE HYDROCHLORIDEREMEDYREPACK INC.20516384-6517-48be-bd6e-718250878a762026-06-25Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 310385
unii: I9W7N6B1KJ
Fluoxetine hydrochlorideFLUOXETINE HYDROCHLORIDEDr.Reddy's Laboratories Limited887fc670-db67-4cfe-967b-46b38375dae52026-06-22Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I9W7N6B1KJ
FluoxetineFLUOXETINEUnit Dose Solutions, Inc.54d9f02c-95ea-99b1-e063-6294a90a91402026-06-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 310385
unii: I9W7N6B1KJ

Reported adverse events (FAERS/openFDA)#

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