Package 0781-1635-10

Brand: isosorbide dinitrate

Generic: isosorbide dinitrate
NDC Package

Package Facts

Identity

Package NDC 0781-1635-10
Digits Only 0781163510
Product NDC 0781-1635
Description

1000 TABLET in 1 BOTTLE (0781-1635-10)

Marketing

Marketing Status
Marketed Since 1988-01-07
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": "9c848a4f-2720-4c80-a0be-e49200cb10f9", "openfda": {"nui": ["N0000175415", "M0014874", "N0000009909"], "upc": ["0307811556017", "0307811695013", "0307811635019"], "unii": ["IA7306519N"], "rxcui": ["206842", "314055", "381056"], "spl_set_id": ["71fdd147-a987-40b6-9f07-82d56525ceb8"], "pharm_class_cs": ["Nitrates [CS]"], "pharm_class_pe": ["Vasodilation [PE]"], "pharm_class_epc": ["Nitrate Vasodilator [EPC]"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0781-1635-01)", "package_ndc": "0781-1635-01", "marketing_start_date": "19880107"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0781-1635-10)", "package_ndc": "0781-1635-10", "marketing_start_date": "19880107"}], "brand_name": "Isosorbide Dinitrate", "product_id": "0781-1635_9c848a4f-2720-4c80-a0be-e49200cb10f9", "dosage_form": "TABLET", "pharm_class": ["Nitrate Vasodilator [EPC]", "Nitrates [CS]", "Vasodilation [PE]"], "product_ndc": "0781-1635", "generic_name": "Isosorbide Dinitrate", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isosorbide Dinitrate", "active_ingredients": [{"name": "ISOSORBIDE DINITRATE", "strength": "5 mg/1"}], "application_number": "ANDA086221", "marketing_category": "ANDA", "marketing_start_date": "19880107", "listing_expiration_date": "20261231"}