Package 84386-106-30

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 84386-106-30
Digits Only 8438610630
Product NDC 84386-106
Product ID 84386-106_a9ed97dd-8041-4a02-889c-dcb8b2805f36
Description

30 TABLET, FILM COATED in 1 BOTTLE (84386-106-30)

Marketing

Marketing Status
Marketed Since 2026-01-15
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": "a9ed97dd-8041-4a02-889c-dcb8b2805f36", "openfda": {"upc": ["0384386106304"], "unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["a9ed97dd-8041-4a02-889c-dcb8b2805f36"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (84386-106-30)", "package_ndc": "84386-106-30", "marketing_start_date": "20260115"}], "brand_name": "Fluoxetine", "product_id": "84386-106_a9ed97dd-8041-4a02-889c-dcb8b2805f36", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "84386-106", "generic_name": "Fluoxetine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA213265", "marketing_category": "ANDA", "marketing_start_date": "20260115", "listing_expiration_date": "20271231"}