Package 65862-079-30

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-079-30
Digits Only 6586207930
Product NDC 65862-079
Description

30 TABLET in 1 BOTTLE (65862-079-30)

Marketing

Marketing Status
Marketed Since 2007-07-02
Brand terbinafine
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8f6e6ae9-4903-4823-b788-de387e8c6fb2", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["6600e2b3-65df-4fc3-8081-d574537d27e3"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-079-01)", "package_ndc": "65862-079-01", "marketing_start_date": "20070702"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-079-30)", "package_ndc": "65862-079-30", "marketing_start_date": "20070702"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-079-99)", "package_ndc": "65862-079-99", "marketing_start_date": "20070702"}], "brand_name": "Terbinafine", "product_id": "65862-079_8f6e6ae9-4903-4823-b788-de387e8c6fb2", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "65862-079", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbinafine", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA078297", "marketing_category": "ANDA", "marketing_start_date": "20070702", "listing_expiration_date": "20261231"}