dipyridamole

Generic: dipyridamole

Labeler: oxford pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dipyridamole
Generic Name dipyridamole
Labeler oxford pharmaceuticals, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

dipyridamole 25 mg/1

Manufacturer
Oxford Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69584-181
Product ID 69584-181_6cf8d202-17fc-4c56-be33-4d74f6591077
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040542
Listing Expiration 2026-12-31
Marketing Start 2021-04-15

Pharmacologic Class

Established (EPC)
platelet aggregation inhibitor [epc]
Physiologic Effect
decreased platelet aggregation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69584181
Hyphenated Format 69584-181

Supplemental Identifiers

RxCUI
197622 309952 309955
UNII
64ALC7F90C
NUI
N0000008832 N0000175578

Packaging Origin

Original Packager
true

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 dipyridamole (source: ndc)
Generic Name dipyridamole (source: ndc)
Application Number ANDA040542 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (69584-181-10)
source: ndc

Packages (1)

69584-181-10 100 TABLET, FILM COATED in 1 BOTTLE (69584-181-10)

Ingredients (1)

dipyridamole (25 mg/1)

Linked Drug Pages (1)

Dipyridamole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6cf8d202-17fc-4c56-be33-4d74f6591077", "openfda": {"nui": ["N0000008832", "N0000175578"], "unii": ["64ALC7F90C"], "rxcui": ["197622", "309952", "309955"], "spl_set_id": ["f7ffd78a-e93a-40f4-8193-2d6ab4dafd00"], "pharm_class_pe": ["Decreased Platelet Aggregation [PE]"], "pharm_class_epc": ["Platelet Aggregation Inhibitor [EPC]"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69584-181-10)", "package_ndc": "69584-181-10", "marketing_start_date": "20210415"}], "brand_name": "Dipyridamole", "product_id": "69584-181_6cf8d202-17fc-4c56-be33-4d74f6591077", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Platelet Aggregation [PE]", "Platelet Aggregation Inhibitor [EPC]"], "product_ndc": "69584-181", "generic_name": "Dipyridamole", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dipyridamole", "active_ingredients": [{"name": "DIPYRIDAMOLE", "strength": "25 mg/1"}], "application_number": "ANDA040542", "marketing_category": "ANDA", "marketing_start_date": "20210415", "listing_expiration_date": "20261231"}