Package 65862-306-12

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 65862-306-12
Digits Only 6586230612
Product NDC 65862-306
Product ID 65862-306_75e37c2c-4f1b-4660-ae32-0ce8106b12ff
Description

120 mL in 1 BOTTLE, GLASS (65862-306-12)

Marketing

Marketing Status
Marketed Since 2009-03-19
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": "75e37c2c-4f1b-4660-ae32-0ce8106b12ff", "openfda": {"upc": ["0365862306128"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310386"], "spl_set_id": ["3195db14-0cae-4b49-9fba-49b869fe92a8"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, GLASS (65862-306-12)", "package_ndc": "65862-306-12", "marketing_start_date": "20090319"}], "brand_name": "Fluoxetine", "product_id": "65862-306_75e37c2c-4f1b-4660-ae32-0ce8106b12ff", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-306", "generic_name": "Fluoxetine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA079209", "marketing_category": "ANDA", "marketing_start_date": "20090319", "listing_expiration_date": "20261231"}