Pantoprazole Sodium Drug For Further Processing
NDC Database

Pantoprazole Sodium Drug For Further Processing

NDC Database

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

DRUG FOR FURTHER PROCESSING 4 Labelers
  • Total Records7
  • NDC7
  • Data SourceFDA
  • Last Marketing Date2013-08-12

35

All
View

28

Bulk Ingredient
View

7

Drug for Further Processing
View
NDC Records (7 records)
2001
01 May
Wasserburger Arzneimittelwerk GmbH
DRUG FOR FURTHER PROCESSING

NDC

62287-923

Labeler

Wasserburger Arzneimittelwerk GmbH

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

INJECTION, POWDER, FOR SOLUTION

Strength

40 mg/1

Start Marketing: 2001-05-01

Substance

PANTOPRAZOLE SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2001-05-01

End Marketing Date

-

Listing / Certification

2026-12-31

2011
01 Sep
DRUG FOR FURTHER PROCESSING

NDC

59746-284

Labeler

JUBILANT CADISTA PHARMACEUTICALS INC.

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, DELAYED RELEASE

Strength

40 mg/1

Start Marketing: 2011-09-01

Substance

PANTOPRAZOLE SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2011-09-01

End Marketing Date

-

Listing / Certification

2026-12-31

2012
28 Sep
DRUG FOR FURTHER PROCESSING

NDC

65862-559

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, DELAYED RELEASE

Strength

20 mg/1

Start Marketing: 2012-09-28

Substance

PANTOPRAZOLE SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-09-28

End Marketing Date

-

Listing / Certification

2027-12-31

2012
28 Sep
DRUG FOR FURTHER PROCESSING

NDC

65862-560

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Pantoprazole Sodium

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, DELAYED RELEASE

Strength

40 mg/1

Start Marketing: 2012-09-28

Substance

PANTOPRAZOLE SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-09-28

End Marketing Date

-

Listing / Certification

2027-12-31

2000
01 May
DRUG FOR FURTHER PROCESSING

NDC

47234-0841

Labeler

Takeda GmbH

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, DELAYED RELEASE

Strength

40 mg/1

Start Marketing: 2000-05-01

Substance

PANTOPRAZOLE SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2000-05-01

End Marketing Date

-

Listing / Certification

2026-12-31

2000
01 May
DRUG FOR FURTHER PROCESSING

NDC

47234-0843

Labeler

Takeda GmbH

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, DELAYED RELEASE

Strength

20 mg/1

Start Marketing: 2000-05-01

Substance

PANTOPRAZOLE SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2000-05-01

End Marketing Date

-

Listing / Certification

2026-12-31

2013
12 Aug
DRUG FOR FURTHER PROCESSING

NDC

47234-0923

Labeler

Takeda GmbH

Nonproprietary Name

PANTOPRAZOLE SODIUM

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

INJECTION, POWDER, FOR SOLUTION

Strength

40 mg/10mL

Start Marketing: 2013-08-12

Substance

PANTOPRAZOLE SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2013-08-12

End Marketing Date

-

Listing / Certification

2026-12-31

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Product Type Breakdown
7 total
  • DRUG FOR FURTHER PROCESSING
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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