NDC 68071-1931

Lisinopril

Lisinopril

Lisinopril is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals, Inc.. The primary component is Lisinopril.

Product ID68071-1931_490fcf48-5478-109d-e054-00144ff8d46c
NDC68071-1931
Product TypeHuman Prescription Drug
Proprietary NameLisinopril
Generic NameLisinopril
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2006-01-13
Marketing CategoryANDA / ANDA
Application NumberANDA077321
Labeler NameNuCare Pharmaceuticals, Inc.
Substance NameLISINOPRIL
Active Ingredient Strength40 mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 68071-1931-9

90 TABLET in 1 BOTTLE (68071-1931-9)
Marketing Start Date2017-02-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68071-1931-5 [68071193105]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-21
Marketing End Date2019-12-31

NDC 68071-1931-9 [68071193109]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-21
Marketing End Date2019-12-31

NDC 68071-1931-3 [68071193103]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-21
Marketing End Date2019-12-31

NDC 68071-1931-6 [68071193106]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-21
Marketing End Date2019-12-31

NDC 68071-1931-8 [68071193108]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-21
Marketing End Date2019-12-31

Drug Details

Active Ingredients

IngredientStrength
LISINOPRIL40 mg/1

OpenFDA Data

SPL SET ID:490fcf48-5477-109d-e054-00144ff8d46c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197884
  • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    0143-1266LisinoprilLisinopril
    0143-1267LisinoprilLisinopril
    0143-1268LisinoprilLisinopril
    0143-1270LisinoprilLisinopril
    0143-9713LisinoprilLisinopril
    0143-9714LisinoprilLisinopril
    0143-9715LisinoprilLisinopril
    0185-0025lisinoprillisinopril
    0185-0101lisinoprillisinopril
    0185-0102lisinoprillisinopril
    0185-0103lisinoprillisinopril
    0185-0104lisinoprillisinopril
    0185-0602lisinoprillisinopril
    0185-0605lisinoprillisinopril
    0185-0610lisinoprillisinopril
    0185-0620lisinoprillisinopril
    0185-0630lisinoprillisinopril
    0185-0640lisinoprillisinopril
    0185-5400lisinoprillisinopril
    0378-2072Lisinoprillisinopril
    0378-2073Lisinoprillisinopril
    0378-2074Lisinoprillisinopril
    0378-2075Lisinoprillisinopril
    0378-2076Lisinoprillisinopril
    68001-270lisinoprillisinopril
    68001-271lisinoprillisinopril
    68001-267lisinoprillisinopril
    68001-272lisinoprillisinopril
    68001-334LisinoprilLisinopril
    68001-268lisinoprillisinopril
    68001-333LisinoprilLisinopril
    68001-335LisinoprilLisinopril
    68001-337LisinoprilLisinopril
    68001-269lisinoprillisinopril
    68001-336LisinoprilLisinopril
    68001-332LisinoprilLisinopril
    68071-1672LISINOPRILLISINOPRIL
    68071-1775LISINOPRILLISINOPRIL
    68071-3064LISINOPRILLISINOPRIL
    68071-1894LISINOPRILLISINOPRIL
    68071-3220LISINOPRILLISINOPRIL
    68071-3113LISINOPRILLISINOPRIL
    68071-3122LISINOPRILLISINOPRIL
    68071-1931LisinoprilLisinopril
    68071-3070lisinoprillisinopril
    68071-3043LISINOPRILLISINOPRIL
    68071-3123LISINOPRILLISINOPRIL
    68071-3145LISINOPRILLISINOPRIL
    68071-3178LISINOPRILLISINOPRIL
    68071-4660LisinoprilLisinopril

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