NDC 65841-664

Dipyridamole

Dipyridamole

Dipyridamole is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Zydus Lifesciences Limited. The primary component is Dipyridamole.

Product ID65841-664_11a26f51-90ef-479a-9c8f-7d9b429982c4
NDC65841-664
Product TypeHuman Prescription Drug
Proprietary NameDipyridamole
Generic NameDipyridamole
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2008-05-22
Marketing CategoryANDA / ANDA
Application NumberANDA040874
Labeler NameZydus Lifesciences Limited
Substance NameDIPYRIDAMOLE
Active Ingredient Strength75 mg/1
Pharm ClassesDecreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 65841-664-01

100 TABLET, FILM COATED in 1 BOTTLE (65841-664-01)
Marketing Start Date2008-05-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65841-664-30 [65841066430]

Dipyridamole TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040874
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-05-22
Marketing End Date2019-12-03

NDC 65841-664-05 [65841066405]

Dipyridamole TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040874
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-05-22

NDC 65841-664-10 [65841066410]

Dipyridamole TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040874
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-05-22

NDC 65841-664-01 [65841066401]

Dipyridamole TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040874
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-05-22

NDC 65841-664-77 [65841066477]

Dipyridamole TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040874
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-05-22

Drug Details

Active Ingredients

IngredientStrength
DIPYRIDAMOLE75 mg/1

OpenFDA Data

SPL SET ID:312aadb1-435c-4aa7-8e46-6506cedacaa0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197622
  • 309952
  • 309955

    • Pharmacological Class

    • Decreased Platelet Aggregation [PE]
    • Platelet Aggregation Inhibitor [EPC]

    NDC Crossover Matching brand name "Dipyridamole" or generic name "Dipyridamole"

    NDCBrand NameGeneric Name
    0115-1070DipyridamoleDIPYRIDAMOLE
    0115-1071DipyridamoleDIPYRIDAMOLE
    0115-1072DipyridamoleDIPYRIDAMOLE
    0404-9852DipyridamoleDipyridamole
    0404-9853DipyridamoleDipyridamole
    0404-9854DipyridamoleDipyridamole
    0527-1461DipyridamoleDipyridamole
    0527-1462DipyridamoleDipyridamole
    0527-1463DipyridamoleDipyridamole
    0615-1573DipyridamoleDipyridamole
    0641-2569DipyridamoleDipyridamole
    51407-626DipyridamoleDipyridamole
    51407-627DipyridamoleDipyridamole
    51407-628DipyridamoleDipyridamole
    51662-1447DIPYRIDAMOLEDIPYRIDAMOLE
    51808-204DipyridamoleDipridamole
    52584-569DipyridamoleDipyridamole
    62559-235DipyridamoleDipyridamole
    62559-236DipyridamoleDipyridamole
    62559-237DipyridamoleDipyridamole
    64980-133DIPYRIDAMOLEDIPYRIDAMOLE
    64980-134DIPYRIDAMOLEDIPYRIDAMOLE
    64980-135DIPYRIDAMOLEDIPYRIDAMOLE
    68151-2996DipyridamoleDipyridamole
    68382-187DipyridamoleDipyridamole
    68382-188DipyridamoleDipyridamole
    68382-189DipyridamoleDipyridamole
    65841-663DipyridamoleDipyridamole
    65841-662DipyridamoleDipyridamole
    65841-664DipyridamoleDipyridamole
    0597-0017Persantinedipyridamole
    0597-0018Persantinedipyridamole
    0597-0019Persantinedipyridamole
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.