fluoxetine
Generic: fluoxetine hydrochloride
Labeler: redpharm drugDrug Facts
Product Profile
Brand Name
fluoxetine
Generic Name
fluoxetine hydrochloride
Labeler
redpharm drug
Dosage Form
CAPSULE
Routes
Active Ingredients
fluoxetine hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67296-1898
Product ID
67296-1898_2c630cea-bfcd-2964-e063-6394a90a15cb
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
672961898
Hyphenated Format
67296-1898
Supplemental Identifiers
RxCUI
UPC
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 (67296-1898-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c630cea-bfcd-2964-e063-6394a90a15cb", "openfda": {"upc": ["0350228115056", "0350228115018", "0350228113106", "0350228115308", "0350228114011", "0350228113014", "0350228114103", "0350228113052"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["0b3da881-475d-cdee-e063-6394a90aee99"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (67296-1898-3)", "package_ndc": "67296-1898-3", "marketing_start_date": "20150316"}], "brand_name": "Fluoxetine", "product_id": "67296-1898_2c630cea-bfcd-2964-e063-6394a90a15cb", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "67296-1898", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Redpharm Drug", "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"}