NDC 52959-728

Lisinopril

Lisinopril

Lisinopril is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Lisinopril.

Product ID52959-728_b6067e83-6c20-4902-84db-cf26f1c3c005
NDC52959-728
Product TypeHuman Prescription Drug
Proprietary NameLisinopril
Generic NameLisinopril
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2005-11-17
Marketing CategoryANDA / ANDA
Application NumberANDA077321
Labeler NameH.J. Harkins Company, Inc.
Substance NameLISINOPRIL
Active Ingredient Strength10 mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 52959-728-90

90 TABLET in 1 BOTTLE (52959-728-90)
Marketing Start Date2005-11-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52959-728-30 [52959072830]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-11-17
Inactivation Date2019-11-13

NDC 52959-728-15 [52959072815]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-11-17
Inactivation Date2019-11-13

NDC 52959-728-90 [52959072890]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-11-17
Inactivation Date2019-11-13

NDC 52959-728-20 [52959072820]

Lisinopril TABLET
Marketing CategoryANDA
Application NumberANDA077321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-11-17
Inactivation Date2019-11-13

Drug Details

Active Ingredients

IngredientStrength
LISINOPRIL10 mg/1

OpenFDA Data

SPL SET ID:033c20a9-c298-4185-a48f-0bf8a2ac918a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 314076
  • 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.