ATORVASTATIN CALCIUM
These highlights do not include all the information needed to use calcium tablets safely and effectively. See full prescribing information for calcium tablets. calcium tablets for oral administration Initial U.S. Approval: 1996
Approved
Approval ID
b18ed051-4081-4978-8414-b6bda877bc41
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 24, 2015
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.
ATORVASTATIN CALCIUM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10544-874
Application NumberANDA090548
Product Classification
M
Marketing Category
C73584
G
Generic Name
ATORVASTATIN CALCIUM
Product Specifications
Route of AdministrationORAL
Effective DateNovember 24, 2015
FDA Product Classification
INGREDIENTS (11)
CALCIUM ACETATEInactive
Code: Y882YXF34X
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
SODIUM CARBONATEInactive
Code: 45P3261C7T
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
HYDROXYPROPYL CELLULOSE (TYPE H)Inactive
Code: RFW2ET671P
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
POLYETHYLENE GLYCOL 8000Inactive
Code: Q662QK8M3B
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATEActive
Quantity: 40 mg in 1 1
Code: YRZ789OWMI
Classification: ACTIM