Package 71205-393-90

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-393-90
Digits Only 7120539390
Product NDC 71205-393
Description

90 CAPSULE in 1 BOTTLE (71205-393-90)

Marketing

Marketing Status
Marketed Since 2020-02-03
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f796fb87-9ffa-4238-a779-5c2268fa41e3", "openfda": {"upc": ["0371205393304"], "unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["ef699ed0-fd9e-4580-93bb-6fd50499dbd1"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-393-30)", "package_ndc": "71205-393-30", "marketing_start_date": "20200203"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-393-60)", "package_ndc": "71205-393-60", "marketing_start_date": "20200203"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-393-90)", "package_ndc": "71205-393-90", "marketing_start_date": "20200203"}], "brand_name": "Fluoxetine", "product_id": "71205-393_f796fb87-9ffa-4238-a779-5c2268fa41e3", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71205-393", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20261231"}