Package 72789-394-90

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-394-90
Digits Only 7278939490
Product NDC 72789-394
Product ID 72789-394_41231fb9-9811-dfe0-e063-6294a90ab664
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-394-90)

Marketing

Marketing Status
Marketed Since 2024-04-16
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": "41231fb9-9811-dfe0-e063-6294a90ab664", "openfda": {"upc": ["0372789394909"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["747fdc13-7c3a-4672-b50c-31c51037bda2"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "42 TABLET in 1 BOTTLE, PLASTIC (72789-394-42)", "package_ndc": "72789-394-42", "marketing_start_date": "20240805"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-394-90)", "package_ndc": "72789-394-90", "marketing_start_date": "20240416"}], "brand_name": "Terbinafine", "product_id": "72789-394_41231fb9-9811-dfe0-e063-6294a90ab664", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "72789-394", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "PD-Rx 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"}