Package 43063-839-90

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 43063-839-90
Digits Only 4306383990
Product NDC 43063-839
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (43063-839-90)

Marketing

Marketing Status
Marketed Since 2018-03-06
Brand fluoxetine
Generic fluoxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32851291-33ce-2831-e063-6294a90a0d3a", "openfda": {"upc": ["0343063839300"], "unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["620ecf00-5473-4420-afd1-94b5b38e7301"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-839-30)", "package_ndc": "43063-839-30", "marketing_start_date": "20160129"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (43063-839-90)", "package_ndc": "43063-839-90", "marketing_start_date": "20180306"}], "brand_name": "Fluoxetine", "product_id": "43063-839_32851291-33ce-2831-e063-6294a90a0d3a", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-839", "generic_name": "Fluoxetine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA090223", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20261231"}