fluoxetine
Generic: fluoxetine hydrochloride
Labeler: medsource pharmaceuticalsDrug Facts
Product Profile
Brand Name
fluoxetine
Generic Name
fluoxetine hydrochloride
Labeler
medsource pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
fluoxetine hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
45865-174
Product ID
45865-174_1302fc08-d5fb-54b4-e063-6394a90a5275
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204597
Listing Expiration
2026-12-31
Marketing Start
2015-03-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
45865174
Hyphenated Format
45865-174
Supplemental Identifiers
RxCUI
UNII
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
ANDA204597 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (45865-174-30)
- 60 CAPSULE in 1 BOTTLE (45865-174-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1302fc08-d5fb-54b4-e063-6394a90a5275", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["1302fc08-d5fa-54b4-e063-6394a90a5275"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (45865-174-30)", "package_ndc": "45865-174-30", "marketing_start_date": "20210908"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (45865-174-60)", "package_ndc": "45865-174-60", "marketing_start_date": "20210415"}], "brand_name": "Fluoxetine", "product_id": "45865-174_1302fc08-d5fb-54b4-e063-6394a90a5275", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "45865-174", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Medsource Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}