Package 16714-112-01

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 16714-112-01
Digits Only 1671411201
Product NDC 16714-112
Product ID 16714-112_a3031cb7-423c-64e2-e1d4-2b07f2e7ba3a
Description

30 TABLET, FILM COATED in 1 BOTTLE (16714-112-01)

Marketing

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

Linked Drug Pages (1)

Fluoxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a3031cb7-423c-64e2-e1d4-2b07f2e7ba3a", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["248642", "313990"], "spl_set_id": ["70b4bd1b-d355-189e-a414-9fff182fd1cd"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-112-01)", "package_ndc": "16714-112-01", "marketing_start_date": "20190918"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-112-02)", "package_ndc": "16714-112-02", "marketing_start_date": "20190918"}], "brand_name": "Fluoxetine", "product_id": "16714-112_a3031cb7-423c-64e2-e1d4-2b07f2e7ba3a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16714-112", "generic_name": "Fluoxetine", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076006", "marketing_category": "ANDA", "marketing_start_date": "20190918", "listing_expiration_date": "20261231"}