NDC 55648-923

ENALAPRIL MALEATE

Enalapril Maleate

ENALAPRIL MALEATE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Wockhardt Limited. The primary component is Enalapril Maleate.

Product ID55648-923_c6ea4a09-66d5-4f33-9f17-9c63cb59e4b5
NDC55648-923
Product TypeHuman Prescription Drug
Proprietary NameENALAPRIL MALEATE
Generic NameEnalapril Maleate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-11
Marketing CategoryANDA / ANDA
Application NumberANDA075483
Labeler NameWockhardt Limited
Substance NameENALAPRIL MALEATE
Active Ingredient Strength3 mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 55648-923-02

100 TABLET in 1 BOTTLE (55648-923-02)
Marketing Start Date2009-12-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55648-923-03 [55648092303]

ENALAPRIL MALEATE TABLET
Marketing CategoryANDA
Application NumberANDA075483
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 55648-923-01 [55648092301]

ENALAPRIL MALEATE TABLET
Marketing CategoryANDA
Application NumberANDA075483
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 55648-923-09 [55648092309]

ENALAPRIL MALEATE TABLET
Marketing CategoryANDA
Application NumberANDA075483
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 55648-923-02 [55648092302]

ENALAPRIL MALEATE TABLET
Marketing CategoryANDA
Application NumberANDA075483
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 55648-923-10 [55648092310]

ENALAPRIL MALEATE TABLET
Marketing CategoryANDA
Application NumberANDA075483
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 55648-923-07 [55648092307]

ENALAPRIL MALEATE TABLET
Marketing CategoryANDA
Application NumberANDA075483
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ENALAPRIL MALEATE2.5 mg/1

OpenFDA Data

SPL SET ID:f1ec6ac1-6b94-40bb-a329-9056f201090c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 858813
  • 858810
  • 858817
  • 858804

    • Pharmacological Class

    • Angiotensin Converting Enzyme Inhibitor [EPC]
    • Angiotensin-converting Enzyme Inhibitors [MoA]
    • Decreased Blood Pressure [PE]

    NDC Crossover Matching brand name "ENALAPRIL MALEATE" or generic name "Enalapril Maleate"

    NDCBrand NameGeneric Name
    0093-0026Enalapril MaleateEnalapril Maleate
    0093-0027Enalapril MaleateEnalapril Maleate
    0093-0028Enalapril MaleateEnalapril Maleate
    0093-0029Enalapril MaleateEnalapril Maleate
    0378-1052Enalapril MaleateEnalapril Maleate
    0615-4589ENALAPRIL MALEATEENALAPRIL MALEATE
    0615-4590ENALAPRIL MALEATEENALAPRIL MALEATE
    0615-4591ENALAPRIL MALEATEENALAPRIL MALEATE
    0615-4593ENALAPRIL MALEATEENALAPRIL MALEATE
    0615-7907Enalapril MaleateEnalapril Maleate
    0615-7908Enalapril MaleateEnalapril Maleate
    0615-7909Enalapril MaleateEnalapril Maleate
    0904-5502ENALAPRIL MALEATEENALAPRIL MALEATE
    0904-5609ENALAPRIL MALEATEENALAPRIL MALEATE
    0904-5610ENALAPRIL MALEATEENALAPRIL MALEATE
    0904-5611ENALAPRIL MALEATEENALAPRIL MALEATE
    10544-170ENALAPRIL MALEATEENALAPRIL MALEATE
    10544-195Enalapril MaleateEnalapril Maleate
    10544-293Enalapril MaleateEnalapril Maleate
    10544-632Enalapril MaleateEnalapril Maleate
    10544-633Enalapril MaleateEnalapril Maleate
    16714-442Enalapril Maleateenalapril maleate
    16714-443Enalapril Maleateenalapril maleate
    16714-444Enalapril Maleateenalapril maleate
    16714-445Enalapril Maleateenalapril maleate
    21695-487ENALAPRIL MALEATEENALAPRIL MALEATE
    21695-488ENALAPRIL MALEATEENALAPRIL MALEATE
    21695-489ENALAPRIL MALEATEENALAPRIL MALEATE
    23155-704Enalapril maleateEnalapril maleate
    68071-1936ENALAPRIL MALEATEENALAPRIL MALEATE
    68071-1938ENALAPRIL MALEATEENALAPRIL MALEATE
    68071-3067Enalapril MaleateEnalapril Maleate
    68071-3303Enalapril MaleateEnalapril Maleate
    68071-3173Enalapril MaleateEnalapril Maleate
    68071-3245Enalapril MaleateEnalapril Maleate
    68071-3221Enalapril MaleateEnalapril Maleate
    68084-390ENALAPRIL MALEATEENALAPRIL MALEATE
    68084-392ENALAPRIL MALEATEENALAPRIL MALEATE
    68084-391ENALAPRIL MALEATEENALAPRIL MALEATE
    68682-710Enalapril MaleateEnalapril Maleate
    68682-712Enalapril MaleateEnalapril Maleate
    68682-711Enalapril MaleateEnalapril Maleate
    68645-457ENALAPRIL MALEATEENALAPRIL MALEATE
    68645-455ENALAPRIL MALEATEENALAPRIL MALEATE
    68645-456ENALAPRIL MALEATEENALAPRIL MALEATE
    68682-713Enalapril MaleateEnalapril Maleate
    68788-7309Enalapril MaleateEnalapril Maleate
    68788-7244Enalapril MaleateEnalapril Maleate
    68788-7275Enalapril MaleateEnalapril Maleate
    68788-9931ENALAPRIL MALEATEENALAPRIL MALEATE
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.