fluoxetine hcl
Generic: fluoxetine hcl
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
fluoxetine hcl
Generic Name
fluoxetine hcl
Labeler
direct_rx
Dosage Form
CAPSULE
Routes
Active Ingredients
fluoxetine hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-656
Product ID
72189-656_4963f68f-8a97-192d-e063-6294a90acb73
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204597
Listing Expiration
2027-12-31
Marketing Start
2026-01-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189656
Hyphenated Format
72189-656
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 hcl (source: ndc)
Generic Name
fluoxetine hcl (source: ndc)
Application Number
ANDA204597 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (72189-656-30)
- 90 CAPSULE in 1 BOTTLE (72189-656-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4963f68f-8a97-192d-e063-6294a90acb73", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["48705e4f-c3ee-af78-e063-6394a90ad052"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-656-30)", "package_ndc": "72189-656-30", "marketing_start_date": "20260115"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-656-90)", "package_ndc": "72189-656-90", "marketing_start_date": "20260115"}], "brand_name": "Fluoxetine HCL", "product_id": "72189-656_4963f68f-8a97-192d-e063-6294a90acb73", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72189-656", "generic_name": "Fluoxetine HCL", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine HCL", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20260115", "listing_expiration_date": "20271231"}