Package 71335-2778-1
Brand: fluoxetine
Generic: fluoxetinePackage Facts
Identity
Package NDC
71335-2778-1
Digits Only
7133527781
Product NDC
71335-2778
Description
30 TABLET, FILM COATED in 1 BOTTLE (71335-2778-1)
Marketing
Marketing Status
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": "b1fb7c4e-9fa8-4fc1-8dae-315e211c5d8f", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313990"], "spl_set_id": ["c1c7ec04-dd9e-400f-8f49-e900945fc61c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2778-1)", "package_ndc": "71335-2778-1", "marketing_start_date": "20251013"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2778-2)", "package_ndc": "71335-2778-2", "marketing_start_date": "20251013"}], "brand_name": "Fluoxetine", "product_id": "71335-2778_b1fb7c4e-9fa8-4fc1-8dae-315e211c5d8f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2778", "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"}