Package 16714-717-01

Brand: entecavir

Generic: entecavir
NDC Package

Package Facts

Identity

Package NDC 16714-717-01
Digits Only 1671471701
Product NDC 16714-717
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-717-01)

Marketing

Marketing Status
Marketed Since 2017-06-15
Brand entecavir
Generic entecavir
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "566171a2-a0b1-4064-88bf-77c9a80bd0f1", "openfda": {"upc": ["0316714718019", "0316714717012"], "unii": ["5968Y6H45M"], "rxcui": ["485434", "485436"], "spl_set_id": ["da705339-c349-444f-a058-4f0cef2864bf"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-717-01)", "package_ndc": "16714-717-01", "marketing_start_date": "20170615"}], "brand_name": "ENTECAVIR", "product_id": "16714-717_566171a2-a0b1-4064-88bf-77c9a80bd0f1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Nucleoside Analog [EXT]", "Nucleoside Reverse Transcriptase Inhibitors [MoA]"], "product_ndc": "16714-717", "generic_name": "ENTECAVIR", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENTECAVIR", "active_ingredients": [{"name": "ENTECAVIR", "strength": ".5 mg/1"}], "application_number": "ANDA206872", "marketing_category": "ANDA", "marketing_start_date": "20170615", "listing_expiration_date": "20261231"}