0228-2620

Generic: isosorbide mononitrate

Labeler: actavis pharma, inc.
NDC Directory DRUG FOR FURTHER PROCESSING DRUG FOR FURTHER PROCESSING Active

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
oral
source: label

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 41667 TABLET in 1 CONTAINER (0228-2620-00)
source: ndc

Packages (1)

Ingredients (1)

isosorbide mononitrate (20 mg/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"}