Package 51655-364-26

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-364-26
Digits Only 5165536426
Product NDC 51655-364
Product ID 51655-364_48eb9f2c-1512-e77b-e063-6394a90a5b31
Description

90 TABLET in 1 BOTTLE (51655-364-26)

Marketing

Marketing Status
Marketed Since 2020-05-28
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": "48eb9f2c-1512-e77b-e063-6394a90a5b31", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["ab6f50a5-87ce-0819-e053-2a95a90a22b7"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (51655-364-26)", "package_ndc": "51655-364-26", "marketing_start_date": "20200528"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "51655-364_48eb9f2c-1512-e77b-e063-6394a90a5b31", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "51655-364", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Northwind Health Company, 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": "20200528", "listing_expiration_date": "20271231"}