Package 72162-1494-3
Brand: fluoxetine hydrochloride
Generic: fluoxetine hydrochloridePackage 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
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"}