Lisinopril
Lisinopril Tablets USP
Approved
Approval ID
6490cffe-28e5-434a-9ff0-81cd37cc9f31
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 16, 2011
Manufacturers
FDA
Legacy Pharmaceutical Packaging
DUNS: 143213275
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Lisinopril
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68645-272
Application NumberANDA076059
Product Classification
M
Marketing Category
C73584
G
Generic Name
Lisinopril
Product Specifications
Route of AdministrationORAL
Effective DateJune 16, 2011
FDA Product Classification
INGREDIENTS (7)
FD&C YELLOW NO. 5Inactive
Code: I753WB2F1M
Classification: IACT
ANHYDROUS DIBASIC CALCIUM PHOSPHATEInactive
Code: L11K75P92J
Classification: IACT
LISINOPRILActive
Quantity: 20 mg in 1 1
Code: E7199S1YWR
Classification: ACTIB
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
MANNITOLInactive
Code: 3OWL53L36A
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
COLLOIDAL SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT