fluoxetine

Generic: fluoxetine hydrochloride

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluoxetine
Generic Name fluoxetine hydrochloride
Labeler bluepoint laboratories
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

fluoxetine hydrochloride 40 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-401
Product ID 68001-401_0c3d632c-6b3e-4e78-e063-6394a90a7ed2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078619
Listing Expiration 2026-12-31
Marketing Start 2019-06-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001401
Hyphenated Format 68001-401

Supplemental Identifiers

RxCUI
310384 310385 313989
UNII
I9W7N6B1KJ

Packaging Origin

Original Packager
true

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
  • 40 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (68001-401-00)
  • 500 CAPSULE in 1 BOTTLE (68001-401-03)
  • 30 CAPSULE in 1 BOTTLE (68001-401-04)
source: ndc

Packages (3)

68001-401-00 100 CAPSULE in 1 BOTTLE (68001-401-00) 68001-401-03 500 CAPSULE in 1 BOTTLE (68001-401-03) 68001-401-04 30 CAPSULE in 1 BOTTLE (68001-401-04)

Ingredients (1)

fluoxetine hydrochloride (40 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": "0c3d632c-6b3e-4e78-e063-6394a90a7ed2", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["f89a5800-6fdb-4938-a28e-3bf1aeb1c21a"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68001-401-00)", "package_ndc": "68001-401-00", "marketing_start_date": "20190619"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (68001-401-03)", "package_ndc": "68001-401-03", "marketing_start_date": "20190619"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68001-401-04)", "package_ndc": "68001-401-04", "marketing_start_date": "20190619"}], "brand_name": "Fluoxetine", "product_id": "68001-401_0c3d632c-6b3e-4e78-e063-6394a90a7ed2", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68001-401", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20190619", "listing_expiration_date": "20261231"}