Package 69452-351-13

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69452-351-13
Digits Only 6945235113
Product NDC 69452-351
Product ID 69452-351_233cb04d-09cc-4312-923f-f4666bdf9754
Description

30 TABLET in 1 BOTTLE, PLASTIC (69452-351-13)

Marketing

Marketing Status
Marketed Since 2022-01-28
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": "233cb04d-09cc-4312-923f-f4666bdf9754", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["34221c17-0d8c-4b56-8af3-c74efab4599e"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (69452-351-13)", "package_ndc": "69452-351-13", "marketing_start_date": "20220128"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (69452-351-20)", "package_ndc": "69452-351-20", "marketing_start_date": "20220128"}], "brand_name": "terbinafine hydrochloride", "product_id": "69452-351_233cb04d-09cc-4312-923f-f4666bdf9754", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "69452-351", "generic_name": "terbinafine hydrochloride", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "terbinafine hydrochloride", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA078163", "marketing_category": "ANDA", "marketing_start_date": "20220128", "listing_expiration_date": "20261231"}