fluoxetine

Generic: fluoxetine hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluoxetine
Generic Name fluoxetine hydrochloride
Labeler aurobindo pharma limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

fluoxetine hydrochloride 40 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-194
Product ID 65862-194_7dd85e52-3c8c-4ca2-b9fa-0dfaed81123e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078619
Marketing Start 2008-01-31
Marketing End 2028-02-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862194
Hyphenated Format 65862-194

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 (65862-194-01)
  • 500 CAPSULE in 1 BOTTLE (65862-194-05)
  • 30 CAPSULE in 1 BOTTLE (65862-194-30)
  • 1000 CAPSULE in 1 BOTTLE (65862-194-99)
source: ndc

Packages (4)

65862-194-01 100 CAPSULE in 1 BOTTLE (65862-194-01) 65862-194-05 500 CAPSULE in 1 BOTTLE (65862-194-05) 65862-194-30 30 CAPSULE in 1 BOTTLE (65862-194-30) 65862-194-99 1000 CAPSULE in 1 BOTTLE (65862-194-99)

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": "7dd85e52-3c8c-4ca2-b9fa-0dfaed81123e", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["45454555-7402-41cb-a452-e6a76e04f387"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (65862-194-01)", "package_ndc": "65862-194-01", "marketing_end_date": "20280229", "marketing_start_date": "20080131"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (65862-194-05)", "package_ndc": "65862-194-05", "marketing_end_date": "20270430", "marketing_start_date": "20080131"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (65862-194-30)", "package_ndc": "65862-194-30", "marketing_end_date": "20280229", "marketing_start_date": "20080131"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (65862-194-99)", "package_ndc": "65862-194-99", "marketing_end_date": "20270228", "marketing_start_date": "20080131"}], "brand_name": "Fluoxetine", "product_id": "65862-194_7dd85e52-3c8c-4ca2-b9fa-0dfaed81123e", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-194", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "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_end_date": "20280229", "marketing_start_date": "20080131"}