Pantoprazole Sodium Bulk Ingredient
NDC Database

Pantoprazole Sodium Bulk Ingredient

NDC Database

National Drug Code (NDC) records including drug products, labelers, dosage forms, strengths, substances and marketing information.

BULK INGREDIENT 26 Labelers
  • Total Records28
  • NDC28
  • Data SourceFDA
  • Last Marketing Date2025-01-15

35

All
View

28

Bulk Ingredient
View

7

Drug for Further Processing
View
NDC Records (28 records)
2021
17 Dec
Azico Biophore India Private Limited
BULK INGREDIENT

NDC

69575-4047

Labeler

Azico Biophore India Private Limited

Nonproprietary Name

Pantoprazole sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

25 kg/25kg

Start Marketing: 2021-12-17

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-17

End Marketing Date

-

Listing / Certification

2026-12-31

2016
01 Jan
Cipla Ltd.
BULK INGREDIENT

NDC

53104-7562

Labeler

Cipla Ltd.

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

40 mg/40mg

Start Marketing: 2016-01-01

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-01-01

End Marketing Date

-

Listing / Certification

2026-12-31

2012
06 Sep
Dr. Reddy's Laboratories Limited
BULK INGREDIENT

NDC

55111-333

Labeler

Dr. Reddy's Laboratories Limited

Nonproprietary Name

Pantoprazole

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, DELAYED RELEASE

Strength

40 mg/1

Start Marketing: 2012-09-06

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-09-06

End Marketing Date

-

Listing / Certification

2026-12-31

2004
20 Jan
Dr.Reddy's Laboratories Limited
BULK INGREDIENT

NDC

55111-051

Labeler

Dr.Reddy's Laboratories Limited

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2004-01-20

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-01-20

End Marketing Date

-

Listing / Certification

2026-12-31

2001
22 Mar
Hetero Drugs Limited
BULK INGREDIENT

NDC

65977-0012

Labeler

Hetero Drugs Limited

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2001-03-22

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-03-22

End Marketing Date

-

Listing / Certification

2026-12-31

2009
03 Nov
Holiday Labs Mexico, S.A. De C.V.
BULK INGREDIENT

NDC

52286-0013

Labeler

Holiday Labs Mexico, S.A. De C.V.

Nonproprietary Name

Pantoprazole Sodium Sesquihydrate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2009-11-03

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-11-03

End Marketing Date

-

Listing / Certification

2027-12-31

2023
15 Oct
IOL Chemicals and Pharmaceuticals Ltd.
BULK INGREDIENT

NDC

49716-334

Labeler

IOL Chemicals and Pharmaceuticals Ltd.

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2023-10-15

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-10-15

End Marketing Date

-

Listing / Certification

2026-12-31

2007
24 Oct
Jubilant Biosys limited
BULK INGREDIENT

NDC

65372-1126

Labeler

Jubilant Biosys limited

Nonproprietary Name

pantoprazole sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2007-10-24

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-10-24

End Marketing Date

-

Listing / Certification

2026-12-31

2024
22 Aug
Matrix Pharmacorp Private Limited
BULK INGREDIENT

NDC

84206-0074

Labeler

Matrix Pharmacorp Private Limited

Nonproprietary Name

PANTOPRAZOLE SODIUM SESQUIHYDRATE

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2024-08-22

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-08-22

End Marketing Date

-

Listing / Certification

2026-12-31

2025
15 Jan
Professional Compounding Centers of America
BULK INGREDIENT

NDC

51927-0354

Labeler

Professional Compounding Centers of America

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2025-01-15

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-01-15

End Marketing Date

-

Listing / Certification

2026-12-31

2021
27 Jul
Professional Compounding Centers of America
BULK INGREDIENT

NDC

51927-5148

Labeler

Professional Compounding Centers of America

Nonproprietary Name

Pantoprazole Sodium Sesquihydrate

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2021-07-27

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-07-27

End Marketing Date

-

Listing / Certification

2027-12-31

2022
01 Apr
PURE AND CURE HEALTHCARE PRIVATE LIMITED
BULK INGREDIENT

NDC

82608-004

Labeler

PURE AND CURE HEALTHCARE PRIVATE LIMITED

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2022-04-01

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-04-01

End Marketing Date

-

Listing / Certification

2026-12-31

2016
01 Jul
Shouguang Fukang Pharmaceuticals Co., Ltd.
BULK INGREDIENT

NDC

64374-008

Labeler

Shouguang Fukang Pharmaceuticals Co., Ltd.

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2016-07-01

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-07-01

End Marketing Date

-

Listing / Certification

2026-12-31

2015
04 Mar
SMS Pharmaceuticals Limited
BULK INGREDIENT

NDC

67835-0007

Labeler

SMS Pharmaceuticals Limited

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2015-03-04

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-03-04

End Marketing Date

-

Listing / Certification

2026-12-31

2015
01 Apr
Spectrum Laboratory Products, Inc.
BULK INGREDIENT

NDC

49452-4972

Labeler

Spectrum Laboratory Products, Inc.

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 g/g

Start Marketing: 2015-04-01

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-04-01

End Marketing Date

-

Listing / Certification

2026-12-31

2014
04 Feb
Srini Pharmaceuticals Private Limited
BULK INGREDIENT

NDC

66174-0038

Labeler

Srini Pharmaceuticals Private Limited

Nonproprietary Name

Pantoprazole Sodium Sesquihydrate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2014-02-04

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-02-04

End Marketing Date

-

Listing / Certification

2026-12-31

2021
14 Jan
SUN PHARMACEUTICAL INDUSTRIES, INC.
BULK INGREDIENT

NDC

62756-128

Labeler

SUN PHARMACEUTICAL INDUSTRIES, INC.

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

25 kg/25kg

Start Marketing: 2021-01-14

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-14

End Marketing Date

-

Listing / Certification

2026-12-31

2002
02 Feb
Vasudha Pharma Chem Limited
BULK INGREDIENT

NDC

66577-020

Labeler

Vasudha Pharma Chem Limited

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2002-02-02

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2002-02-02

End Marketing Date

-

Listing / Certification

2027-12-31

2024
11 Apr
BULK INGREDIENT

NDC

59651-953

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Pantoprazole Sodium Process-II

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

50 kg/50kg

Start Marketing: 2024-04-11

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-04-11

End Marketing Date

-

Listing / Certification

2026-12-31

2023
04 Nov
BULK INGREDIENT

NDC

65862-426

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Pantoprazole Sodium Sesquihydrate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

50 kg/50kg

Start Marketing: 2023-11-04

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-11-04

End Marketing Date

-

Listing / Certification

2026-12-31

2022
19 May
BULK INGREDIENT

NDC

62207-981

Labeler

Granules India Ltd

Nonproprietary Name

Pantoprazole Sodium Sesquihydrate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

15 kg/15kg

Start Marketing: 2022-05-19

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-05-19

End Marketing Date

-

Listing / Certification

2026-12-31

2014
20 Mar
BULK INGREDIENT

NDC

49632-160

Labeler

PMC Isochem

Nonproprietary Name

PANTOPRAZOLE SODIUM SESQUIHYDRATE

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2014-03-20

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-03-20

End Marketing Date

-

Listing / Certification

2026-12-31

2018
23 Jan
BULK INGREDIENT

NDC

42765-001

Labeler

METROCHEM API PRIVATE LIMITED

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2018-01-23

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-01-23

End Marketing Date

-

Listing / Certification

2026-12-31

2010
23 Jul
BULK INGREDIENT

NDC

68069-0005

Labeler

Moehs Cantabra SL

Nonproprietary Name

Pantoprazole Sodium Sesquihydrate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2010-07-23

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-07-23

End Marketing Date

-

Listing / Certification

2026-12-31

2010
26 Mar
BULK INGREDIENT

NDC

14501-0025

Labeler

MSN Laboratories Private Limited

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2010-03-26

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-03-26

End Marketing Date

-

Listing / Certification

2026-12-31

2019
09 Sep
BULK INGREDIENT

NDC

72640-008

Labeler

MSN Life Sciences Private Limited

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2019-09-09

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-09-09

End Marketing Date

-

Listing / Certification

2026-12-31

2016
21 Jan
BULK INGREDIENT

NDC

63850-3210

Labeler

Natco Pharma Limited

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2016-01-21

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-01-21

End Marketing Date

-

Listing / Certification

2026-12-31

2003
01 Jan
BULK INGREDIENT

NDC

53069-0770

Labeler

Quimica Sintetica S.A.

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2003-01-01

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing / Certification

2026-12-31

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Product Type Breakdown
28 total
  • BULK INGREDIENT
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

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