Package 72189-243-30

Brand: terbinafine

Generic: terbinafine
NDC Package

Package Facts

Identity

Package NDC 72189-243-30
Digits Only 7218924330
Product NDC 72189-243
Product ID 72189-243_2c28596f-8fc8-42e5-e063-6294a90a0ad6
Description

30 TABLET in 1 BOTTLE (72189-243-30)

Marketing

Marketing Status
Marketed Since 2021-07-23
Brand terbinafine
Generic terbinafine
Sample Package No

Linked Drug Pages (1)

TERBINAFINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c28596f-8fc8-42e5-e063-6294a90a0ad6", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["c7cf55e2-f637-e2d9-e053-2995a90a6270"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-243-30)", "package_ndc": "72189-243-30", "marketing_start_date": "20210723"}], "brand_name": "TERBINAFINE", "product_id": "72189-243_2c28596f-8fc8-42e5-e063-6294a90a0ad6", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "72189-243", "generic_name": "TERBINAFINE", "labeler_name": "direct rx", "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": "20210723", "listing_expiration_date": "20261231"}