fluoxetine

Generic: fluoxetine

Labeler: qpharma inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluoxetine
Generic Name fluoxetine
Labeler qpharma inc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

fluoxetine hydrochloride 20 mg/1

Manufacturer
QPharma Inc

Identifiers & Regulatory

Product NDC 42708-025
Product ID 42708-025_45b407ca-52ca-b229-e063-6394a90ab9fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076001
Listing Expiration 2026-12-31
Marketing Start 2002-01-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42708025
Hyphenated Format 42708-025

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 (source: ndc)
Application Number ANDA076001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (42708-025-30)
source: ndc

Packages (1)

42708-025-30 30 CAPSULE in 1 BOTTLE (42708-025-30)

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": "45b407ca-52ca-b229-e063-6394a90ab9fd", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["b4831735-6731-473a-b4f0-1f4a67aa7120"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 CAPSULE in 1 BOTTLE (42708-025-30)", "package_ndc": "42708-025-30", "marketing_start_date": "20180314"}], "brand_name": "Fluoxetine", "product_id": "42708-025_45b407ca-52ca-b229-e063-6394a90ab9fd", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42708-025", "generic_name": "Fluoxetine", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076001", "marketing_category": "ANDA", "marketing_start_date": "20020129", "listing_expiration_date": "20261231"}