NDC 63629-7663

Fosinopril Sodium

Fosinopril

Fosinopril Sodium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Fosinopril Sodium.

Product ID63629-7663_83380dad-e764-4efe-b670-3949ae6b0e83
NDC63629-7663
Product TypeHuman Prescription Drug
Proprietary NameFosinopril Sodium
Generic NameFosinopril
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-06-16
Marketing CategoryANDA / ANDA
Application NumberANDA077222
Labeler NameBryant Ranch Prepack
Substance NameFOSINOPRIL SODIUM
Active Ingredient Strength10 mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 63629-7663-1

30 TABLET in 1 BOTTLE (63629-7663-1)
Marketing Start Date2016-06-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-7663-5 [63629766305]

Fosinopril Sodium TABLET
Marketing CategoryANDA
Application NumberANDA077222
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-16
Inactivation Date2020-01-31

NDC 63629-7663-1 [63629766301]

Fosinopril Sodium TABLET
Marketing CategoryANDA
Application NumberANDA077222
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-16
Inactivation Date2020-01-31

NDC 63629-7663-3 [63629766303]

Fosinopril Sodium TABLET
Marketing CategoryANDA
Application NumberANDA077222
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-16
Inactivation Date2020-01-31

NDC 63629-7663-2 [63629766302]

Fosinopril Sodium TABLET
Marketing CategoryANDA
Application NumberANDA077222
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-16
Inactivation Date2020-01-31

NDC 63629-7663-7 [63629766307]

Fosinopril Sodium TABLET
Marketing CategoryANDA
Application NumberANDA077222
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-16
Inactivation Date2020-01-31

NDC 63629-7663-6 [63629766306]

Fosinopril Sodium TABLET
Marketing CategoryANDA
Application NumberANDA077222
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-16
Inactivation Date2020-01-31

NDC 63629-7663-4 [63629766304]

Fosinopril Sodium TABLET
Marketing CategoryANDA
Application NumberANDA077222
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-16
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FOSINOPRIL SODIUM10 mg/1

OpenFDA Data

SPL SET ID:07efdd18-956e-4aca-af46-cde86f44709c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 857169
  • 857187

    • Pharmacological Class

    • Angiotensin Converting Enzyme Inhibitor [EPC]
    • Angiotensin-converting Enzyme Inhibitors [MoA]

    NDC Crossover Matching brand name "Fosinopril Sodium" or generic name "Fosinopril"

    NDCBrand NameGeneric Name
    0093-7222Fosinopril SodiumFosinopril Sodium
    0093-7223Fosinopril SodiumFosinopril Sodium
    0093-7224Fosinopril SodiumFosinopril Sodium
    0185-0041Fosinopril SodiumFosinopril Sodium
    0185-0042Fosinopril SodiumFosinopril Sodium
    0185-0047Fosinopril SodiumFosinopril Sodium
    16571-770Fosinopril SodiumFosinopril Sodium
    16571-771Fosinopril SodiumFosinopril Sodium
    16571-772Fosinopril SodiumFosinopril Sodium
    31722-200Fosinopril SodiumFosinopril Sodium
    31722-201Fosinopril SodiumFosinopril Sodium
    31722-202Fosinopril SodiumFosinopril Sodium
    43353-870Fosinopril sodiumFosinopril sodium
    43547-386Fosinopril sodiumfosinopirl sodium
    43547-387Fosinopril sodiumfosinopril sodium
    43547-388Fosinopril sodiumfosinopril sodium
    50090-0890Fosinopril SodiumFosinopril Sodium
    50090-1112Fosinopril SodiumFosinopril Sodium
    50090-1504Fosinopril SodiumFosinopril Sodium
    50090-2500Fosinopril SodiumFosinopril
    50090-2977Fosinopril SodiumFosinopril
    50090-3428Fosinopril sodiumFosinopril sodium
    50090-3444Fosinopril sodiumFosinopril sodium
    50090-3780Fosinopril sodiumfosinopirl sodium
    50090-4743Fosinopril sodiumfosinopril sodium
    50268-327Fosinopril sodiumfosinopirl sodium
    50268-328Fosinopril sodiumfosinopril sodium
    50268-329Fosinopril sodiumfosinopril sodium
    50436-0274Fosinopril SodiumFosinopril Sodium
    50436-3138Fosinopril SodiumFosinopril Sodium
    53217-277Fosinopril sodiumFosinopril sodium
    53217-278Fosinopril sodiumFosinopril sodium
    63629-5279Fosinopril SodiumFosinopril Sodium
    63629-6994Fosinopril SodiumFosinopril Sodium
    63629-7293Fosinopril SodiumFosinopril
    68258-6106Fosinopril SodiumFosinopril Sodium
    68788-7333Fosinopril sodiumFosinopril sodium
    69097-856Fosinopril SodiumFosinopril Sodium
    69097-857Fosinopril SodiumFosinopril Sodium
    69097-858Fosinopril SodiumFosinopril Sodium
    71335-0187Fosinopril SodiumFosinopril Sodium
    71335-0381Fosinopril SodiumFosinopril Sodium
    71335-0726Fosinopril sodiumFosinopril sodium
    71335-0873Fosinopril SodiumFosinopril Sodium
    76282-202Fosinopril sodiumFosinopril sodium
    76282-200Fosinopril sodiumFosinopril sodium
    76282-201Fosinopril sodiumFosinopril sodium
    63629-7663Fosinopril SodiumFosinopril Sodium
    65862-471Fosinopril SodiumFosinopril Sodium
    65862-473Fosinopril SodiumFosinopril Sodium
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