Package 16714-114-01

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-114-01
Digits Only 1671411401
Product NDC 16714-114
Product ID 16714-114_e90468ef-aee3-2684-3a9d-7bd58919e9de
Description

30 TABLET, FILM COATED in 1 BOTTLE (16714-114-01)

Marketing

Marketing Status
Marketed Since 2019-09-18
Brand fluoxetine hydrochloride
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluoxetine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "ORAL"], "spl_id": "e90468ef-aee3-2684-3a9d-7bd58919e9de", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["1f8b1834-d5d7-72b6-d2ed-cb074344d59e"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-114-01)", "package_ndc": "16714-114-01", "marketing_start_date": "20190918"}], "brand_name": "Fluoxetine hydrochloride", "product_id": "16714-114_e90468ef-aee3-2684-3a9d-7bd58919e9de", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16714-114", "generic_name": "Fluoxetine hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211721", "marketing_category": "ANDA", "marketing_start_date": "20190918", "listing_expiration_date": "20261231"}