Package 50090-3575-0
Brand: terbinafine
Generic: terbinafine hydrochloridePackage Facts
Identity
Package NDC
50090-3575-0
Digits Only
5009035750
Product NDC
50090-3575
Description
30 TABLET in 1 BOTTLE (50090-3575-0)
Marketing
Marketing Status
Brand
terbinafine
Generic
terbinafine hydrochloride
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d94fe835-d140-489d-853a-cbd1c0d6a62d", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["5de4c245-7086-453b-b90a-7a1242ec2c0b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-3575-0)", "package_ndc": "50090-3575-0", "marketing_start_date": "20180910"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (50090-3575-1)", "package_ndc": "50090-3575-1", "marketing_start_date": "20141128"}], "brand_name": "Terbinafine", "product_id": "50090-3575_d94fe835-d140-489d-853a-cbd1c0d6a62d", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "50090-3575", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}