Package 68788-7450-1

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-7450-1
Digits Only 6878874501
Product NDC 68788-7450
Product ID 68788-7450_f92d2c6c-a52a-4251-bdfc-4d6f8a668dc7
Description

100 TABLET in 1 BOTTLE (68788-7450-1)

Marketing

Marketing Status
Marketed Since 2019-12-27
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": "f92d2c6c-a52a-4251-bdfc-4d6f8a668dc7", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["085e0809-6b7f-447e-976e-8276c29daad6"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7450-1)", "package_ndc": "68788-7450-1", "marketing_start_date": "20191227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7450-3)", "package_ndc": "68788-7450-3", "marketing_start_date": "20191227"}], "brand_name": "Terbinafine", "product_id": "68788-7450_f92d2c6c-a52a-4251-bdfc-4d6f8a668dc7", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "68788-7450", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Preferred 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"}