Package 72162-1494-3

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1494-3
Digits Only 7216214943
Product NDC 72162-1494
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1494-3)

Marketing

Marketing Status
Marketed Since 2023-10-04
Brand fluoxetine hydrochloride
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fceae5a4-c99c-437f-8874-d7ebe9378e3b", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313990"], "spl_set_id": ["d4043133-38de-4faa-bb76-8fafa5913844"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1494-1)", "package_ndc": "72162-1494-1", "marketing_start_date": "20231004"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1494-3)", "package_ndc": "72162-1494-3", "marketing_start_date": "20231004"}], "brand_name": "fluoxetine hydrochloride", "product_id": "72162-1494_fceae5a4-c99c-437f-8874-d7ebe9378e3b", "dosage_form": "TABLET, COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-1494", "generic_name": "fluoxetine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203836", "marketing_category": "ANDA", "marketing_start_date": "20160822", "listing_expiration_date": "20261231"}