NDC 0071-0156

Lipitor

Atorvastatin Calcium

Lipitor is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Parke-davis Div Of Pfizer Inc. The primary component is Atorvastatin Calcium Trihydrate.

• Product ID: 0071-0156_0ba214c6-250e-42a0-aea8-5e44aba04882
• NDC: 0071-0156
• Product Type: Human Prescription Drug
• Proprietary Name: Lipitor
• Generic Name: Atorvastatin Calcium
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 1996-12-17
• Marketing Category: NDA / NDA
• Application Number: NDA020702
• Labeler Name: Parke-Davis Div of Pfizer Inc
• Substance Name: ATORVASTATIN CALCIUM TRIHYDRATE
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0071-0156-10

1000 TABLET, FILM COATED in 1 BOTTLE (0071-0156-10)

• Marketing Start Date: 1996-12-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0071-0156-94 [00071015694]

Lipitor TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA020702
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-12-17
• Marketing End Date: 2016-02-26

NDC 0071-0156-23 [00071015623]

Lipitor TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA020702
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-12-17

NDC 0071-0156-96 [00071015696]

Lipitor TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA020702
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1996-12-17

NDC 0071-0156-10 [00071015610]

Lipitor TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA020702
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1996-12-17

NDC 0071-0156-40 [00071015640]

Lipitor TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA020702
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-12-17

Drug Details

Active Ingredients

Ingredient	Strength
ATORVASTATIN CALCIUM TRIHYDRATE	20 mg/1

OpenFDA Data

• SPL SET ID: c6e131fe-e7df-4876-83f7-9156fc4e8228
• Manufacturer:
  • Parke-Davis Div of Pfizer Inc
• UNII:
  • 48A5M73Z4Q
• RxNorm Concept Unique ID - RxCUI:
  • 259255
  • 617318
  • 262095
  • 617310
  • 617311
  • 617312
  • 617314
  • 617320
• UPC Code:
  • 0300710155237
  • 0300710156234
  • 0300710157231
  • 0300710158238

Pharmacological Class

• HMG-CoA Reductase Inhibitor [EPC]
• Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

NDC Crossover Matching brand name "Lipitor" or generic name "Atorvastatin Calcium"

NDC	Brand Name	Generic Name
0071-0155	Lipitor	atorvastatin calcium
0071-0156	Lipitor	atorvastatin calcium
0071-0157	Lipitor	atorvastatin calcium
0071-0158	Lipitor	atorvastatin calcium
70518-0036	Lipitor	Lipitor
21695-255	Lipitor	Lipitor
49299-1090	LIPITOR	LIPITOR
49299-1091	LIPITOR	LIPITOR
49299-1092	LIPITOR	LIPITOR
49299-1093	LIPITOR	LIPITOR
55289-861	Lipitor	Lipitor
55289-870	Lipitor	Lipitor
55289-800	Lipitor	Lipitor
63629-1446	Lipitor	Lipitor
63629-6768	Lipitor	Lipitor
63629-1447	Lipitor	Lipitor
63629-6776	Lipitor	Lipitor
63629-6633	Lipitor	Lipitor