Package 69097-859-07
Brand: terbinafine
Generic: terbinafinePackage Facts
Identity
Package NDC
69097-859-07
Digits Only
6909785907
Product NDC
69097-859
Description
100 TABLET in 1 BOTTLE (69097-859-07)
Marketing
Marketing Status
Brand
terbinafine
Generic
terbinafine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3db8f4b-ea51-41b6-859e-ad91677aaf73", "openfda": {"upc": ["0369097859022"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["18b16aad-1877-4b07-b532-f0ef4843af91"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (69097-859-02)", "package_ndc": "69097-859-02", "marketing_start_date": "20160627"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (69097-859-07)", "package_ndc": "69097-859-07", "marketing_start_date": "20160627"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69097-859-12)", "package_ndc": "69097-859-12", "marketing_start_date": "20160627"}], "brand_name": "Terbinafine", "product_id": "69097-859_e3db8f4b-ea51-41b6-859e-ad91677aaf73", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "69097-859", "generic_name": "Terbinafine", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbinafine", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077533", "marketing_category": "ANDA", "marketing_start_date": "20160627", "listing_expiration_date": "20261231"}