Package 68071-4873-3

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4873-3
Digits Only 6807148733
Product NDC 68071-4873
Product ID 68071-4873_1ae1cc9d-0253-361f-e063-6394a90a966b
Description

30 TABLET in 1 BOTTLE (68071-4873-3)

Marketing

Marketing Status
Marketed Since 2019-04-29
Brand terbinafine
Generic terbinafine hydrochloride
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": "1ae1cc9d-0253-361f-e063-6394a90a966b", "openfda": {"upc": ["0368071487336"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["87af930f-493c-590e-e053-2a95a90a804a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4873-3)", "package_ndc": "68071-4873-3", "marketing_start_date": "20190429"}], "brand_name": "Terbinafine", "product_id": "68071-4873_1ae1cc9d-0253-361f-e063-6394a90a966b", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "68071-4873", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,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": "20070702", "listing_expiration_date": "20261231"}