LORAZEPAM
LORAZEPAM tablet
Approved
Approval ID
3af556f7-3d8c-4079-b6bc-5051966e5f3b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 10, 2011
Manufacturers
FDA
RedPharm Drug Inc.
DUNS: 008039641
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
lorazepam
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67296-0306
Application NumberANDA072927
Product Classification
M
Marketing Category
C73584
G
Generic Name
lorazepam
Product Specifications
Route of AdministrationORAL
Effective DateMay 20, 2011
FDA Product Classification
INGREDIENTS (5)
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
LORAZEPAMActive
Quantity: 1 mg in 1 1
Code: O26FZP769L
Classification: ACTIB
LACTOSEInactive
Code: J2B2A4N98G
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
POLACRILIN POTASSIUMInactive
Code: 0BZ5A00FQU
Classification: IACT