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.

NDC Product Code67296-0306

Application NumberANDA072927

Marketing CategoryC73584

Route of AdministrationORAL

Effective DateMay 20, 2011

Generic Namelorazepam

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