Package 68071-1640-3

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-1640-3
Digits Only 6807116403
Product NDC 68071-1640
Product ID 68071-1640_1d4de36f-4f9b-4e7a-e063-6294a90a4b3a
Description

30 TABLET in 1 BOTTLE (68071-1640-3)

Marketing

Marketing Status
Marketed Since 2017-11-02
Brand terbinafine hydrochloride
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Terbinafine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d4de36f-4f9b-4e7a-e063-6294a90a4b3a", "openfda": {"upc": ["0368071164039"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["5d01fde5-e4cf-6670-e053-2991aa0a5b15"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-1640-3)", "package_ndc": "68071-1640-3", "marketing_start_date": "20171102"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "68071-1640_1d4de36f-4f9b-4e7a-e063-6294a90a4b3a", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "68071-1640", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,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": "20140813", "listing_expiration_date": "20261231"}