fluoxetine

Generic: fluoxetine hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluoxetine
Generic Name fluoxetine hydrochloride
Labeler northwind health company, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

fluoxetine hydrochloride 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-100
Product ID 51655-100_46e3219e-b656-3d59-e063-6394a90aa00a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078619
Listing Expiration 2027-12-31
Marketing Start 2014-05-20

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655100
Hyphenated Format 51655-100

Supplemental Identifiers

RxCUI
310385
UNII
I9W7N6B1KJ

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name fluoxetine (source: ndc)
Generic Name fluoxetine hydrochloride (source: ndc)
Application Number ANDA078619 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (51655-100-26)
  • 30 CAPSULE in 1 BOTTLE, DISPENSING (51655-100-52)
source: ndc

Packages (2)

51655-100-26 90 CAPSULE in 1 BOTTLE, PLASTIC (51655-100-26) 51655-100-52 30 CAPSULE in 1 BOTTLE, DISPENSING (51655-100-52)

Ingredients (1)

fluoxetine hydrochloride (20 mg/1)

Linked Drug Pages (1)

Fluoxetine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46e3219e-b656-3d59-e063-6394a90aa00a", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["cb66a702-7670-4a73-98fb-0e63151a1ffb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (51655-100-26)", "package_ndc": "51655-100-26", "marketing_start_date": "20220830"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, DISPENSING (51655-100-52)", "package_ndc": "51655-100-52", "marketing_start_date": "20140520"}], "brand_name": "Fluoxetine", "product_id": "51655-100_46e3219e-b656-3d59-e063-6394a90aa00a", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-100", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20140520", "listing_expiration_date": "20271231"}