Package 70710-1149-1

Brand: isosorbide dinitrate

Generic: isosorbide dinitrate
NDC Package

Package Facts

Identity

Package NDC 70710-1149-1
Digits Only 7071011491
Product NDC 70710-1149
Description

100 TABLET in 1 BOTTLE (70710-1149-1)

Marketing

Marketing Status
Marketed Since 2019-11-25
Brand isosorbide dinitrate
Generic isosorbide dinitrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "60a0c153-add8-44d9-a2f1-4c333d0eb42d", "openfda": {"nui": ["N0000175415", "M0014874", "N0000009909"], "upc": ["0370710114916"], "unii": ["IA7306519N"], "rxcui": ["197839", "197840", "206842", "314055", "381056"], "spl_set_id": ["16818b32-ee5e-4e07-b848-31e892c4b98a"], "pharm_class_cs": ["Nitrates [CS]"], "pharm_class_pe": ["Vasodilation [PE]"], "pharm_class_epc": ["Nitrate Vasodilator [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70710-1149-0)", "package_ndc": "70710-1149-0", "marketing_start_date": "20191125"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1149-1)", "package_ndc": "70710-1149-1", "marketing_start_date": "20191125"}], "brand_name": "Isosorbide dinitrate", "product_id": "70710-1149_60a0c153-add8-44d9-a2f1-4c333d0eb42d", "dosage_form": "TABLET", "pharm_class": ["Nitrate Vasodilator [EPC]", "Nitrates [CS]", "Vasodilation [PE]"], "product_ndc": "70710-1149", "generic_name": "Isosorbide dinitrate", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isosorbide dinitrate", "active_ingredients": [{"name": "ISOSORBIDE DINITRATE", "strength": "10 mg/1"}], "application_number": "ANDA213057", "marketing_category": "ANDA", "marketing_start_date": "20191125", "listing_expiration_date": "20261231"}