Isosorbide Dinitrate
Generic: isosorbide dinitrate
Labeler: McKesson Corporation dba SKY PackagingDrug Facts
Product Profile
Brand Name
Isosorbide Dinitrate
Generic Name
isosorbide dinitrate
Labeler
McKesson Corporation dba SKY Packaging
Dosage Form
TABLET
Routes
Active Ingredients
ISOSORBIDE DINITRATE 10 mg/1
Identifiers & Regulatory
Product NDC
63739-569
Product ID
63739-569_2a324bbb-569b-c73e-e063-6294a90addfe
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA086925
Marketing Start
1979-12-22
Marketing End
2026-02-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63739569
Hyphenated Format
63739-569
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
Isosorbide Dinitrate (source: ndc)
Generic Name
isosorbide dinitrate (source: ndc)
Application Number
ANDA086925 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-569-10) / 10 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a324bbb-569b-c73e-e063-6294a90addfe", "openfda": {"nui": ["N0000175415", "M0014874", "N0000009909"], "unii": ["IA7306519N"], "rxcui": ["206842", "381056"], "spl_set_id": ["b334fcb9-9b54-44f7-b708-82c13fbe2035"], "pharm_class_cs": ["Nitrates [CS]"], "pharm_class_pe": ["Vasodilation [PE]"], "pharm_class_epc": ["Nitrate Vasodilator [EPC]"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-569-10) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "63739-569-10", "marketing_end_date": "20260228", "marketing_start_date": "20151130"}], "brand_name": "Isosorbide Dinitrate", "product_id": "63739-569_2a324bbb-569b-c73e-e063-6294a90addfe", "dosage_form": "TABLET", "pharm_class": ["Nitrate Vasodilator [EPC]", "Nitrates [CS]", "Vasodilation [PE]"], "product_ndc": "63739-569", "generic_name": "isosorbide dinitrate", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isosorbide Dinitrate", "active_ingredients": [{"name": "ISOSORBIDE DINITRATE", "strength": "10 mg/1"}], "application_number": "ANDA086925", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "19791222"}