Package 0904-7345-61

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7345-61
Digits Only 0904734561
Product NDC 0904-7345
Product ID 0904-7345_6cb4d9cd-a5c3-43da-a5ed-4659b864c9cc
Description

100 BLISTER PACK in 1 CARTON (0904-7345-61) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-01-03
Brand fluoxetine
Generic fluoxetine hydrochloride
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": "6cb4d9cd-a5c3-43da-a5ed-4659b864c9cc", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385"], "spl_set_id": ["76b264ce-2a13-4511-8e21-4ffad0a327f9"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7345-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7345-61", "marketing_start_date": "20250103"}], "brand_name": "Fluoxetine", "product_id": "0904-7345_6cb4d9cd-a5c3-43da-a5ed-4659b864c9cc", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0904-7345", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20250103", "listing_expiration_date": "20261231"}