fluoxetine hydrochloride

Product NDC
49884-336
11-digit product format
498840336
Labeler code
49884
Product ID
49884-336_71c75730-de24-4bfe-ad24-c92107cd5b74
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fluoxetine hydrochloride
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Endo USA, Inc.
Application
ANDA203836
Marketing category
ANDA
Marketing start
2016-08-22
Substance
FLUOXETINE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
fluoxetine hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FLUOXETINE HYDROCHLORIDE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiI9W7N6B1KJ
Rxcui248642, 313990

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce7d40ce-bfb8-ee15-a060-423ec90d7ac9Product name620250331
e5b459e3-ddce-4802-aab4-2c901d71ae85Product name520250129
6d3d5b3a-d6b8-8417-8428-6414b08f1464Product name320240130
e7177a8f-11de-ee90-ca22-068e6ef54cf5Product name420230104
82da1192-6e97-fa73-2f85-6a50c10b4704Product name320161212
877783eb-030c-6e3f-0979-804cf94d8856Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49884-336-01fluoxetine hydrochloride100 in 1 BOTTLE, PLASTICTABLET, COATED10020
49884-336-10fluoxetine hydrochloride1000 in 1 BOTTLE, PLASTICTABLET, COATED100020
49884-336-11fluoxetine hydrochloride30 in 1 BOTTLE, PLASTICTABLET, COATED3020
49884-336-82fluoxetine hydrochloride2000 in 1 BOTTLE, PLASTICTABLET, COATED200020

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49884-336-01EA - Each49884-33660dcd4f1-a8cd-46da-bbf2-658523b2b8ad12016-09-02
49884-336-11EA - Each49884-33667c21752-fc62-417f-91d3-de3e58832f6a12016-09-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49884-336FLUOXETINE HYDROCHLORIDE TABLET, COATED [ENDO USA, INC.]20Current NDC, Legacy NDC, 4 package rows20250109_53ac797d-8792-4a8c-9708-d1de3d377e8f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
248642FLUoxetine 20 MG Oral TabletPSN4afdf87f-462b-4a38-9c0d-e74995c492ea104
248642fluoxetine 20 MG Oral TabletSCD4afdf87f-462b-4a38-9c0d-e74995c492ea104
248642fluoxetine 20 MG (as fluoxetine hydrochloride 22.4 MG) Oral TabletSY4afdf87f-462b-4a38-9c0d-e74995c492ea104
248642FLUoxetine 20 MG Oral TabletPSN72e391aa-1a46-4589-8550-f83ac9241cf1103
248642fluoxetine 20 MG Oral TabletSCD72e391aa-1a46-4589-8550-f83ac9241cf1103
248642fluoxetine 20 MG (as fluoxetine hydrochloride 22.4 MG) Oral TabletSY72e391aa-1a46-4589-8550-f83ac9241cf1103
248642FLUoxetine 20 MG Oral TabletPSNa04a5bed-d051-4bb4-ae20-b09b10d5c181102
248642fluoxetine 20 MG Oral TabletSCDa04a5bed-d051-4bb4-ae20-b09b10d5c181102
248642fluoxetine 20 MG (as fluoxetine hydrochloride 22.4 MG) Oral TabletSYa04a5bed-d051-4bb4-ae20-b09b10d5c181102
248642FLUoxetine 20 MG Oral TabletPSNda785a8a-d897-494e-9fd2-1d09b32f0190101
248642fluoxetine 20 MG Oral TabletSCDda785a8a-d897-494e-9fd2-1d09b32f0190101
248642fluoxetine 20 MG (as fluoxetine hydrochloride 22.4 MG) Oral TabletSYda785a8a-d897-494e-9fd2-1d09b32f0190101
248642FLUoxetine 20 MG Oral TabletPSN53ac797d-8792-4a8c-9708-d1de3d377e8f20
313990FLUoxetine HCl 10 MG Oral TabletPSN53ac797d-8792-4a8c-9708-d1de3d377e8f20
313990fluoxetine 10 MG Oral TabletSCD53ac797d-8792-4a8c-9708-d1de3d377e8f20
248642fluoxetine 20 MG Oral TabletSCD53ac797d-8792-4a8c-9708-d1de3d377e8f20
313990fluoxetine 10 MG (as fluoxetine hydrochloride 11.2 MG) Oral TabletSY53ac797d-8792-4a8c-9708-d1de3d377e8f20
248642fluoxetine 20 MG (as fluoxetine hydrochloride 22.4 MG) Oral TabletSY53ac797d-8792-4a8c-9708-d1de3d377e8f20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
49884-336-0149884033601100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-01) 2016-08-220000-00-00NoNoCurrent
49884-336-10498840336101000 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-10) 2016-08-220000-00-00NoNoCurrent
49884-336-114988403361130 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-11) 2016-08-220000-00-00NoNoCurrent
49884-336-82498840336822000 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-82) 2016-08-220000-00-00NoNoCurrent