NDC 64764-046

Prevacid

Lansoprazole

Prevacid is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Takeda Pharmaceuticals America, Inc.. The primary component is Lansoprazole.

• Product ID: 64764-046_04bc4bc3-3191-4283-81f6-efdb0693af01
• NDC: 64764-046
• Product Type: Human Prescription Drug
• Proprietary Name: Prevacid
• Generic Name: Lansoprazole
• Dosage Form: Capsule, Delayed Release
• Route of Administration: ORAL
• Marketing Start Date: 1995-05-10
• Marketing Category: NDA / NDA
• Application Number: NDA020406
• Labeler Name: Takeda Pharmaceuticals America, Inc.
• Substance Name: LANSOPRAZOLE
• Active Ingredient Strength: 30 mg/1
• Pharm Classes: Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 64764-046-06

5 BLISTER PACK in 1 TRAY (64764-046-06) > 4 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

• Marketing Start Date: 1995-05-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 64764-046-30 [64764004630]

Prevacid CAPSULE, DELAYED RELEASE

• Marketing Category: NDA
• Application Number: NDA020406
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-08-09
• Marketing End Date: 2010-10-22

NDC 64764-046-19 [64764004619]

Prevacid CAPSULE, DELAYED RELEASE

• Marketing Category: NDA
• Application Number: NDA020406
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1995-05-10

NDC 64764-046-11 [64764004611]

Prevacid CAPSULE, DELAYED RELEASE

• Marketing Category: NDA
• Application Number: NDA020406
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1995-05-10

NDC 64764-046-13 [64764004613]

Prevacid CAPSULE, DELAYED RELEASE

• Marketing Category: NDA
• Application Number: NDA020406
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1995-05-10

NDC 64764-046-06 [64764004606]

Prevacid CAPSULE, DELAYED RELEASE

• Marketing Category: NDA
• Application Number: NDA020406
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1995-05-10

Drug Details

Active Ingredients

Ingredient	Strength
LANSOPRAZOLE	30 mg/1

OpenFDA Data

• SPL SET ID: 71ba78cb-7e46-43eb-9425-fa130f537f84
• Manufacturer:
  • Takeda Pharmaceuticals America, Inc.
• UNII:
  • 0K5C5T2QPG
• RxNorm Concept Unique ID - RxCUI:
  • 351261
  • 351260
  • 866152
  • 596843
  • 206206
  • 206205
  • 596918
  • 311277
• UPC Code:
  • 0364764046132

Pharmacological Class

• Proton Pump Inhibitor [EPC]
• Proton Pump Inhibitors [MoA]
• Inhibition Gastric Acid Secretion [PE]
• Proton Pump Inhibitor [EPC]
• Proton Pump Inhibitors [MoA]
• Inhibition Gastric Acid Secretion [PE]

Medicade Reported Pricing

64764004613 PREVACID DR 30 MG CAPSULE

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Prevacid" or generic name "Lansoprazole"

NDC	Brand Name	Generic Name
0067-6286	Prevacid	Lansoprazole
70518-0502	Prevacid	Prevacid
49999-480	Prevacid	Prevacid
55154-0253	Prevacid	Prevacid
55289-704	Prevacid	Prevacid
63629-3352	Prevacid	Prevacid
64764-046	Prevacid	Prevacid
64764-541	Prevacid	Prevacid
0113-7003	Basic Care Lansoprazole	Lansoprazole
0113-7116	basic care lansoprazole	Lansoprazole
0113-0116	Good Sense Lansoprazole	Lansoprazole
0113-0117	Good Sense lansoprazole	Lansoprazole
0113-1114	Good Sense Lansoprazole	Lansoprazole
0093-3008	Lansoprazole	Lansoprazole
0093-3009	Lansoprazole	Lansoprazole
0093-7350	Lansoprazole	Lansoprazole
0093-7351	Lansoprazole	Lansoprazole
0113-6002	Prevacid 24 HR	lansoprazole