LISINOPRIL
Lisinopril Tablets USP2.5 mg, 5 mg, 10 mg, 20 mg, 30 mg and 40 mg
Approved
Approval ID
c7d18687-9a6b-4d56-8d16-3830ad17cb8d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 8, 2010
Manufacturers
FDA
Blenheim Pharmacal, Inc.
DUNS: 171434587
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 Code10544-240
Application NumberANDA077321
Product Classification
M
Marketing Category
C73584
G
Generic Name
LISINOPRIL
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 8, 2010
FDA Product Classification
INGREDIENTS (7)
LISINOPRILActive
Quantity: 40 mg in 1 1
Code: E7199S1YWR
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
ANHYDROUS DIBASIC CALCIUM PHOSPHATEInactive
Code: L11K75P92J
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
MANNITOLInactive
Code: 3OWL53L36A
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
FERRIC OXIDE YELLOWInactive
Code: EX438O2MRT
Classification: IACT