Package 62135-709-90
Brand: isoniazid
Generic: isoniazidPackage Facts
Identity
Package NDC
62135-709-90
Digits Only
6213570990
Product NDC
62135-709
Description
90 TABLET in 1 BOTTLE (62135-709-90)
Marketing
Marketing Status
Brand
isoniazid
Generic
isoniazid
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2df7a936-6840-66cc-e063-6294a90ae096", "openfda": {"nui": ["N0000175483"], "upc": ["0362135709907"], "unii": ["V83O1VOZ8L"], "rxcui": ["197832"], "spl_set_id": ["2e09b1a5-9786-427f-bf00-be15b06eb7e7"], "pharm_class_epc": ["Antimycobacterial [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-709-90)", "package_ndc": "62135-709-90", "marketing_start_date": "20231020"}], "brand_name": "Isoniazid", "product_id": "62135-709_2df7a936-6840-66cc-e063-6294a90ae096", "dosage_form": "TABLET", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "62135-709", "generic_name": "Isoniazid", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoniazid", "active_ingredients": [{"name": "ISONIAZID", "strength": "300 mg/1"}], "application_number": "ANDA089776", "marketing_category": "ANDA", "marketing_start_date": "19880613", "listing_expiration_date": "20261231"}