NDC 70518-0701

LISINOPRIL

Lisinopril

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

Product ID70518-0701_5b37ad88-ff4a-4d29-e053-2991aa0aed65
NDC70518-0701
Product TypeHuman Prescription Drug
Proprietary NameLISINOPRIL
Generic NameLisinopril
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-08-18
Marketing CategoryANDA / ANDA
Application NumberANDA076164
Labeler NameREMEDYREPACK INC.
Substance NameLISINOPRIL
Active Ingredient Strength30 mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 70518-0701-0

90 TABLET in 1 BOTTLE, PLASTIC (70518-0701-0)
Marketing Start Date2017-08-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0701-0 [70518070100]

LISINOPRIL TABLET
Marketing CategoryANDA
Application NumberANDA076164
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-08-18

NDC 70518-0701-1 [70518070101]

LISINOPRIL TABLET
Marketing CategoryANDA
Application NumberANDA076164
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-10

Drug Details

Active Ingredients

IngredientStrength
LISINOPRIL30 mg/1

OpenFDA Data

SPL SET ID:9ad3e0be-8520-4a8a-a10d-0e3ade75489d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 205326

    • 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.