Package 43353-893-16

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43353-893-16
Digits Only 4335389316
Product NDC 43353-893
Product ID 43353-893_280bbc43-14a1-47e0-a702-8cd8117c2978
Description

6000 TABLET in 1 BOTTLE (43353-893-16)

Marketing

Marketing Status
Marketed Since 2014-02-26
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": "280bbc43-14a1-47e0-a702-8cd8117c2978", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["808dab18-43f1-4895-a023-edbde722863e"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "6000 TABLET in 1 BOTTLE (43353-893-16)", "package_ndc": "43353-893-16", "marketing_start_date": "20140226"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "43353-893_280bbc43-14a1-47e0-a702-8cd8117c2978", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "43353-893", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbinafine Hydrochloride", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077714", "marketing_category": "ANDA", "marketing_start_date": "20120822", "listing_expiration_date": "20261231"}