fluoxetine
Generic: fluoxetine
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
fluoxetine
Generic Name
fluoxetine
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
fluoxetine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-5930
Product ID
63629-5930_4b756a64-ce57-4db2-b70f-681d542a1133
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208698
Listing Expiration
2026-12-31
Marketing Start
2017-04-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636295930
Hyphenated Format
63629-5930
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 (source: ndc)
Application Number
ANDA208698 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-5930-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b756a64-ce57-4db2-b70f-681d542a1133", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313990"], "spl_set_id": ["ada19ae4-f3bd-47fa-a5c3-a6bb3aa34943"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-5930-1)", "package_ndc": "63629-5930-1", "marketing_start_date": "20250602"}], "brand_name": "Fluoxetine", "product_id": "63629-5930_4b756a64-ce57-4db2-b70f-681d542a1133", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63629-5930", "generic_name": "Fluoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208698", "marketing_category": "ANDA", "marketing_start_date": "20170407", "listing_expiration_date": "20261231"}