Package 51672-5306-2

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51672-5306-2
Digits Only 5167253062
Product NDC 51672-5306
Product ID 51672-5306_135b375a-b00e-72c3-e063-6394a90af4f3
Description

500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2)

Marketing

Marketing Status
Marketed Since 2019-02-15
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"], "spl_id": "135b375a-b00e-72c3-e063-6394a90af4f3", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["77b6ae48-8e3a-42e6-9b5a-aeed750861e8"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2)", "package_ndc": "51672-5306-2", "marketing_start_date": "20190215"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51672-5306-6)", "package_ndc": "51672-5306-6", "marketing_start_date": "20190215"}], "brand_name": "FLUOXETINE HYDROCHLORIDE", "product_id": "51672-5306_135b375a-b00e-72c3-e063-6394a90af4f3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51672-5306", "generic_name": "FLUOXETINE HYDROCHLORIDE", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUOXETINE HYDROCHLORIDE", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211477", "marketing_category": "ANDA", "marketing_start_date": "20190215", "listing_expiration_date": "20261231"}