"0071-0157-23" National Drug Code (NDC)

NDC Code	0071-0157-23
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (0071-0157-23)
Product NDC	0071-0157
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lipitor
Non-Proprietary Name	Atorvastatin Calcium
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	19961217
End Marketing Date	20260331
Marketing Category Name	NDA
Application Number	NDA020702
Manufacturer	Parke-Davis Div of Pfizer Inc
Substance Name	ATORVASTATIN CALCIUM TRIHYDRATE
Strength	40
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]