fluoxetine
Generic: fluoxetine hydrochloride
Labeler: calvin scott & co., inc.Drug Facts
Product Profile
Brand Name
fluoxetine
Generic Name
fluoxetine hydrochloride
Labeler
calvin scott & co., inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
fluoxetine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
17224-171
Product ID
17224-171_f709b80f-6425-790e-e053-6394a90a17fc
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
17224171
Hyphenated Format
17224-171
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
- 10 mg/1
Packaging
- 21 CAPSULE in 1 BOTTLE (17224-171-21)
- 30 CAPSULE in 1 BOTTLE (17224-171-30)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f709b80f-6425-790e-e053-6394a90a17fc", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["3453755b-3ed6-47a3-b4c7-c64758e7784c"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (17224-171-21)", "package_ndc": "17224-171-21", "marketing_start_date": "20150316"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (17224-171-30)", "package_ndc": "17224-171-30", "marketing_start_date": "20150316"}], "brand_name": "Fluoxetine", "product_id": "17224-171_f709b80f-6425-790e-e053-6394a90a17fc", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "17224-171", "generic_name": "FLUOXETINE HYDROCHLORIDE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}