Package 69097-731-02

Brand: terbinafine hydrochloride

Generic: terbinafine tablets 250 mg
NDC Package

Package Facts

Identity

Package NDC 69097-731-02
Digits Only 6909773102
Product NDC 69097-731
Description

30 TABLET in 1 BOTTLE (69097-731-02)

Marketing

Marketing Status
Marketed Since 2021-01-08
Brand terbinafine hydrochloride
Generic terbinafine tablets 250 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "feb4ee13-5f95-4a62-8395-55bad95c424b", "openfda": {"upc": ["0369097731021"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["daf41866-6f2b-4483-b575-456becd6e85f"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (69097-731-02)", "package_ndc": "69097-731-02", "marketing_start_date": "20210108"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (69097-731-07)", "package_ndc": "69097-731-07", "marketing_start_date": "20210108"}], "brand_name": "TERBINAFINE HYDROCHLORIDE", "product_id": "69097-731_feb4ee13-5f95-4a62-8395-55bad95c424b", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "69097-731", "generic_name": "Terbinafine Tablets 250 mg", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TERBINAFINE HYDROCHLORIDE", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077137", "marketing_category": "ANDA", "marketing_start_date": "20210108", "listing_expiration_date": "20261231"}