Package 70000-0338-1

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70000-0338-1
Digits Only 7000003381
Product NDC 70000-0338
Description

1 TUBE in 1 CARTON (70000-0338-1) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2018-07-30
Brand terbinafine hydrochloride
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "39854f19-d8c0-6438-e063-6394a90a9422", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["992528"], "spl_set_id": ["a9412747-c7f9-4242-91ed-3695f372f6c9"], "manufacturer_name": ["Cardinal Health, 110 dba LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70000-0338-1)  / 15 g in 1 TUBE", "package_ndc": "70000-0338-1", "marketing_start_date": "20180730"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "70000-0338_39854f19-d8c0-6438-e063-6394a90a9422", "dosage_form": "CREAM", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "70000-0338", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Cardinal Health, 110 dba LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Terbinafine Hydrochloride", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "ANDA077511", "marketing_category": "ANDA", "marketing_start_date": "20180730", "listing_expiration_date": "20261231"}