NDC 50090-3763

LISINOPRIL

Lisinopril

LISINOPRIL is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Lisinopril.

Product ID50090-3763_1cc2a3c0-75b0-428b-9fed-f7813d9a343f
NDC50090-3763
Product TypeHuman Prescription Drug
Proprietary NameLISINOPRIL
Generic NameLisinopril
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2011-11-01
Marketing CategoryANDA / ANDA
Application NumberANDA076164
Labeler NameA-S Medication Solutions
Substance NameLISINOPRIL
Active Ingredient Strength40 mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 50090-3763-0

30 TABLET in 1 BOTTLE (50090-3763-0)
Marketing Start Date2018-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-3763-2 [50090376302]

LISINOPRIL TABLET
Marketing CategoryANDA
Application NumberANDA076164
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28

NDC 50090-3763-0 [50090376300]

LISINOPRIL TABLET
Marketing CategoryANDA
Application NumberANDA076164
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-11-01

NDC 50090-3763-1 [50090376301]

LISINOPRIL TABLET
Marketing CategoryANDA
Application NumberANDA076164
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-09-30

Drug Details

Active Ingredients

IngredientStrength
LISINOPRIL40 mg/1

OpenFDA Data

SPL SET ID:a881df2d-e3b7-413f-b4bb-2c3d917b0811
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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.