Package 63187-233-90

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 63187-233-90
Digits Only 6318723390
Product NDC 63187-233
Product ID 63187-233_d8af1a25-3072-4c46-a287-61f19bb7b5c9
Description

90 CAPSULE in 1 BOTTLE (63187-233-90)

Marketing

Marketing Status
Marketed Since 2002-01-29
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": "d8af1a25-3072-4c46-a287-61f19bb7b5c9", "openfda": {"upc": ["0363187233907"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["1a2a5194-b793-4c62-a177-040dad38526b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (63187-233-90)", "package_ndc": "63187-233-90", "marketing_start_date": "20020129"}], "brand_name": "Fluoxetine", "product_id": "63187-233_d8af1a25-3072-4c46-a287-61f19bb7b5c9", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63187-233", "generic_name": "Fluoxetine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076001", "marketing_category": "ANDA", "marketing_start_date": "20020129", "listing_expiration_date": "20261231"}