0228-2620
Generic: isosorbide mononitrate
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
isosorbide mononitrate
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Active Ingredients
isosorbide mononitrate 20 mg/1
Identifiers & Regulatory
Product NDC
0228-2620
Product ID
0228-2620_cdf0c4d2-2425-49ea-b8a8-f08fa1188cf7
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2023-02-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02282620
Hyphenated Format
0228-2620
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 mononitrate (source: label)
Generic Name
isosorbide mononitrate (source: ndc)
Application Number
ANDA075037 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 41667 TABLET in 1 CONTAINER (0228-2620-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "cdf0c4d2-2425-49ea-b8a8-f08fa1188cf7", "openfda": {}, "finished": false, "packaging": [{"description": "41667 TABLET in 1 CONTAINER (0228-2620-00)", "package_ndc": "0228-2620-00", "marketing_start_date": "07-FEB-23"}], "product_id": "0228-2620_cdf0c4d2-2425-49ea-b8a8-f08fa1188cf7", "dosage_form": "TABLET", "product_ndc": "0228-2620", "generic_name": "Isosorbide Mononitrate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "ISOSORBIDE MONONITRATE", "strength": "20 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20230207", "listing_expiration_date": "20261231"}