Package 70518-3907-2

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3907-2
Digits Only 7051839072
Product NDC 70518-3907
Product ID 70518-3907_3ba00ff4-7c5d-64a8-e063-6394a90a2608
Description

45 TABLET in 1 BOTTLE, PLASTIC (70518-3907-2)

Marketing

Marketing Status
Marketed Since 2024-05-09
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": "3ba00ff4-7c5d-64a8-e063-6394a90a2608", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["2886b2ff-815f-4621-bc28-1fea082c1920"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE, PLASTIC (70518-3907-2)", "package_ndc": "70518-3907-2", "marketing_start_date": "20240509"}], "brand_name": "terbinafine hydrochloride", "product_id": "70518-3907_3ba00ff4-7c5d-64a8-e063-6394a90a2608", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "70518-3907", "generic_name": "terbinafine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "terbinafine hydrochloride", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA078163", "marketing_category": "ANDA", "marketing_start_date": "20231103", "listing_expiration_date": "20261231"}