fluoxetine
Generic: fluoxetine hydrochloride
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
fluoxetine
Generic Name
fluoxetine hydrochloride
Labeler
cardinal health 107, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
fluoxetine hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55154-2638
Product ID
55154-2638_97385230-4710-47cf-9617-fc0f2fef78b3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078619
Listing Expiration
2026-12-31
Marketing Start
2024-12-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551542638
Hyphenated Format
55154-2638
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
ANDA078619 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 10 BLISTER PACK in 1 BAG (55154-2638-0) / 1 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "97385230-4710-47cf-9617-fc0f2fef78b3", "openfda": {"upc": ["0055154263801"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["06394c4b-99f4-4257-bf29-53c170c5a061"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2638-0) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "55154-2638-0", "marketing_start_date": "20241204"}], "brand_name": "Fluoxetine", "product_id": "55154-2638_97385230-4710-47cf-9617-fc0f2fef78b3", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55154-2638", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20241204", "listing_expiration_date": "20261231"}