NDC 0003-0894

ELIQUIS

Apixaban

ELIQUIS is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by E.r. Squibb & Sons, L.l.c.. The primary component is Apixaban.

• Product ID: 0003-0894_07ff3e00-b2de-4323-b48e-46e90e682e69
• NDC: 0003-0894
• Product Type: Human Prescription Drug
• Proprietary Name: ELIQUIS
• Generic Name: Apixaban
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2012-12-28
• Marketing Category: NDA / NDA
• Application Number: NDA202155
• Labeler Name: E.R. Squibb & Sons, L.L.C.
• Substance Name: APIXABAN
• Active Ingredient Strength: 5 mg/1
• Pharm Classes: Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0003-0894-21

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0003-0894-21)

• Marketing Start Date: 2012-12-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0003-0894-70 [00003089470]

ELIQUIS TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA202155
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-06-01

NDC 0003-0894-21 [00003089421]

ELIQUIS TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA202155
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-12-28

NDC 0003-0894-31 [00003089431]

ELIQUIS TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA202155
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-12-28

NDC 0003-0894-91 [00003089491]

ELIQUIS TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA202155
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-12-28

NDC 0003-0894-41 [00003089441]

ELIQUIS TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA202155
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-12-28
• Marketing End Date: 2017-06-01

Drug Details

Active Ingredients

Ingredient	Strength
APIXABAN	5 mg/1

OpenFDA Data

• SPL SET ID: e9481622-7cc6-418a-acb6-c5450daae9b0
• Manufacturer:
  • E.R. Squibb & Sons, L.L.C.
• UNII:
  • 3Z9Y7UWC1J
• RxNorm Concept Unique ID - RxCUI:
  • 1364435
  • 1992427
  • 1992428
  • 1364445
  • 1364447
  • 1364441
• UPC Code:
  • 0300030893215

Pharmacological Class

• Factor Xa Inhibitor [EPC]
• Factor Xa Inhibitors [MoA]

NDC Crossover Matching brand name "ELIQUIS" or generic name "Apixaban"

NDC	Brand Name	Generic Name
0003-0893	ELIQUIS	apixaban
0003-0894	ELIQUIS	apixaban
0003-3764	ELIQUIS	apixaban
50090-1436	ELIQUIS	apixaban
50090-1437	ELIQUIS	apixaban
55154-0612	ELIQUIS	apixaban
70518-1861	ELIQUIS	ELIQUIS
55154-0613	ELIQUIS	ELIQUIS
63629-7747	ELIQUIS	ELIQUIS
67296-1673	ELIQUIS	ELIQUIS
14445-149	apixaban	apixaban
14445-150	apixaban	apixaban