Package 71335-2784-1

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 71335-2784-1
Digits Only 7133527841
Product NDC 71335-2784
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2784-1)

Marketing

Marketing Status
Marketed Since 2025-08-18
Brand fluoxetine
Generic fluoxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "545ff7d3-04a5-43a2-9417-f35a6c5a892b", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313990"], "spl_set_id": ["97e7929f-dec4-467d-93c2-93360884e9e9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2784-1)", "package_ndc": "71335-2784-1", "marketing_start_date": "20250818"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2784-2)", "package_ndc": "71335-2784-2", "marketing_start_date": "20250818"}], "brand_name": "Fluoxetine", "product_id": "71335-2784_545ff7d3-04a5-43a2-9417-f35a6c5a892b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2784", "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": "ANDA213286", "marketing_category": "ANDA", "marketing_start_date": "20200408", "listing_expiration_date": "20261231"}