Package 71335-2785-1

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 71335-2785-1
Digits Only 7133527851
Product NDC 71335-2785
Product ID 71335-2785_f197b0ee-0e93-4639-9c5a-17cff936b036
Description

100 TABLET in 1 BOTTLE (71335-2785-1)

Marketing

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

Linked Drug Pages (1)

FLUOXETINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f197b0ee-0e93-4639-9c5a-17cff936b036", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["248642"], "spl_set_id": ["651e8c32-4519-4619-854f-4be03c6240b6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2785-1)", "package_ndc": "71335-2785-1", "marketing_start_date": "20250818"}], "brand_name": "FLUOXETINE", "product_id": "71335-2785_f197b0ee-0e93-4639-9c5a-17cff936b036", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2785", "generic_name": "fluoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUOXETINE", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA212684", "marketing_category": "ANDA", "marketing_start_date": "20240812", "listing_expiration_date": "20261231"}