Package 70518-2941-0

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2941-0
Digits Only 7051829410
Product NDC 70518-2941
Product ID 70518-2941_4ab97e93-0067-21d7-e063-6294a90ae00d
Description

30 TABLET in 1 BLISTER PACK (70518-2941-0)

Marketing

Marketing Status
Marketed Since 2020-11-13
Brand terbinafine
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4ab97e93-0067-21d7-e063-6294a90ae00d", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["44c6f6e7-e0c0-450e-83ce-1ed4f3efddec"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2941-0)", "package_ndc": "70518-2941-0", "marketing_start_date": "20201113"}], "brand_name": "Terbinafine", "product_id": "70518-2941_4ab97e93-0067-21d7-e063-6294a90ae00d", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "70518-2941", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20201113", "listing_expiration_date": "20271231"}