Clopidogrel Bisulfate - NDC Database

NDC Database
24 labelers
Clopidogrel Bisulfate

Clopidogrel Bisulfate

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

DRUG FOR FURTHER PROCESSINGBULK INGREDIENT

Browse NDC

28
All
25
Bulk Ingredient
3
Drug for Further Processing
Last Marketing Date
2026-05-20
Data Source
FDA
First Marketing Date
1997-11-17
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NDC Records Timeline (28 records)
Clear
2012
17 May
Apotex Corp.
DRUG FOR FURTHER PROCESSING

NDC

60505-3992

Labeler

Apotex Corp.

Nonproprietary Name

clopidogrel bisulfate

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, FILM COATED

Strength

75 mg/1

Start Marketing: 2012-05-17

Substance

CLOPIDOGREL BISULFATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-05-17

End Marketing Date

-

Listing / Certification

2026-12-31

2023
10 Jan
ARENE LIFE SCIENCES PRIVATE LIMITED
BULK INGREDIENT

NDC

71859-002

Labeler

ARENE LIFE SCIENCES PRIVATE LIMITED

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2023-01-10

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-01-10

End Marketing Date

-

Listing / Certification

2027-12-31

2023
17 May
AX Pharmaceutical Corp
BULK INGREDIENT

NDC

73377-236

Labeler

AX Pharmaceutical Corp

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

1 g/g

Start Marketing: 2023-05-17

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-05-17

End Marketing Date

-

Listing / Certification

2026-12-31

2023
25 Apr
Chemeca Drugs Private Limited
BULK INGREDIENT

NDC

77777-109

Labeler

Chemeca Drugs Private Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

50 kg/50kg

Start Marketing: 2023-04-25

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-04-25

End Marketing Date

-

Listing / Certification

2026-12-31

2019
15 Feb
Chemeca Drugs Private Limited
BULK INGREDIENT

NDC

77777-109

Labeler

Chemeca Drugs Private Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

2 kg/2kg

Start Marketing: 2019-02-15

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-02-15

End Marketing Date

-

Listing / Certification

2026-12-31

2017
01 Jun
Darmerica, LLC
BULK INGREDIENT

NDC

71052-296

Labeler

Darmerica, LLC

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 g/g

Start Marketing: 2017-06-01

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-06-01

End Marketing Date

-

Listing / Certification

2027-12-31

2013
20 Mar
Dr. Reddy's Laboratories Limited
BULK INGREDIENT

NDC

55111-032

Labeler

Dr. Reddy's Laboratories Limited

Nonproprietary Name

Clopidogrel Bisulphate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2013-03-20

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-03-20

End Marketing Date

-

Listing / Certification

2026-12-31

2020
30 Dec
Dr. Reddy's Laboratories Limited
BULK INGREDIENT

NDC

71796-027

Labeler

Dr. Reddy's Laboratories Limited

Nonproprietary Name

Clopidogrel bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2020-12-30

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-12-30

End Marketing Date

-

Listing / Certification

2026-12-31

1997
17 Nov
Hetero Drugs Limited
BULK INGREDIENT

NDC

65977-0037

Labeler

Hetero Drugs Limited

Nonproprietary Name

Clopidogrel

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 1997-11-17

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1997-11-17

End Marketing Date

-

Listing / Certification

2026-12-31

2023
15 Oct
IOL Chemicals and Pharmaceuticals Ltd.
BULK INGREDIENT

NDC

49716-329

Labeler

IOL Chemicals and Pharmaceuticals Ltd.

Nonproprietary Name

CLOPIDOGREL BISULFATE

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2023-10-15

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-10-15

End Marketing Date

-

Listing / Certification

2026-12-31

2011
10 Jan
Jubilant Biosys limited
BULK INGREDIENT

NDC

65372-1150

Labeler

Jubilant Biosys limited

Nonproprietary Name

clopidogrel bisulphate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2011-01-10

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-01-10

End Marketing Date

-

Listing / Certification

2026-12-31

2015
15 May
MSN Organics Private Limited
BULK INGREDIENT

NDC

50379-0015

Labeler

MSN Organics Private Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2015-05-15

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-05-15

End Marketing Date

-

Listing / Certification

2026-12-31

2026
20 May
PRAVEEN LABORATORIES PRIVATE LIMITED
BULK INGREDIENT

NDC

87307-002

Labeler

PRAVEEN LABORATORIES PRIVATE LIMITED

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2026-05-20

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-05-20

End Marketing Date

-

Listing / Certification

2027-12-31

2012
27 Feb
Sanofi Winthrop Industrie
DRUG FOR FURTHER PROCESSING

NDC

53360-1171

Labeler

Sanofi Winthrop Industrie

Nonproprietary Name

clopidogrel bisulfate

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, FILM COATED

Strength

75 mg/1

Start Marketing: 2012-02-27

Substance

CLOPIDOGREL BISULFATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-02-27

End Marketing Date

-

Listing / Certification

2026-12-31

2025
31 Mar
SUN PHARMACEUTICAL INDUSTRIES, INC.
BULK INGREDIENT

NDC

62756-965

Labeler

SUN PHARMACEUTICAL INDUSTRIES, INC.

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

25 kg/25kg

Start Marketing: 2025-03-31

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-03-31

End Marketing Date

-

Listing / Certification

2026-12-31

2018
01 Dec
Vasudha Pharma Chem Limited
BULK INGREDIENT

NDC

66577-037

Labeler

Vasudha Pharma Chem Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2018-12-01

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-01

End Marketing Date

-

Listing / Certification

2027-12-31

2011
25 Sep
Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
BULK INGREDIENT

NDC

12666-0019

Labeler

Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2011-09-25

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-09-25

End Marketing Date

-

Listing / Certification

2026-12-31

2015
29 Jun
Zhejiang Charioteer Phamaceutical Co., Ltd.
BULK INGREDIENT

NDC

63310-2440

Labeler

Zhejiang Charioteer Phamaceutical Co., Ltd.

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

25 kg/25kg

Start Marketing: 2015-06-29

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-06-29

End Marketing Date

-

Listing / Certification

2026-12-31

2011
09 Feb
ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
BULK INGREDIENT

NDC

64220-103

Labeler

ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2011-02-09

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-02-09

End Marketing Date

-

Listing / Certification

2026-12-31

2020
18 Nov
Zhejiang Lepu Pharmaceutical Co., Ltd.
BULK INGREDIENT

NDC

68578-0014

Labeler

Zhejiang Lepu Pharmaceutical Co., Ltd.

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2020-11-18

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-11-18

End Marketing Date

-

Listing / Certification

2026-12-31

2019
30 Oct
BULK INGREDIENT

NDC

68166-005

Labeler

QIDONG DONGYUE PHARMACEUTICAL CO., LTD.

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2019-10-30

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-10-30

End Marketing Date

-

Listing / Certification

2026-12-31

2024
11 Jan
BULK INGREDIENT

NDC

59651-398

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Clopidogrel Bisulfate (Form II)

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

50 kg/50kg

Start Marketing: 2024-01-11

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-11

End Marketing Date

-

Listing / Certification

2026-12-31

2012
17 May
DRUG FOR FURTHER PROCESSING

NDC

65862-357

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, FILM COATED

Strength

75 mg/1

Start Marketing: 2012-05-17

Substance

CLOPIDOGREL BISULFATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-05-17

End Marketing Date

-

Listing / Certification

2026-12-31

2024
17 Jan
BULK INGREDIENT

NDC

65862-372

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

50 kg/50kg

Start Marketing: 2024-01-17

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-17

End Marketing Date

-

Listing / Certification

2026-12-31

2020
17 Jan
BULK INGREDIENT

NDC

42765-004

Labeler

Metrochem API Private Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

25 kg/25kg

Start Marketing: 2020-01-17

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-17

End Marketing Date

-

Listing / Certification

2026-12-31

2010
31 Mar
BULK INGREDIENT

NDC

14501-0026

Labeler

MSN Laboratories Private Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2010-03-31

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-03-31

End Marketing Date

-

Listing / Certification

2026-12-31

2019
30 Oct
BULK INGREDIENT

NDC

72640-009

Labeler

MSN Life Sciences Private Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2019-10-30

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-10-30

End Marketing Date

-

Listing / Certification

2026-12-31

2001
13 Nov
BULK INGREDIENT

NDC

50787-0022

Labeler

Signa S.A. de C.V.

Nonproprietary Name

CLOPIDOGREL

Marketing Category

BULK INGREDIENT

Dosage Form

POWDER

Strength

1 kg/kg

Start Marketing: 2001-11-13

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-11-13

End Marketing Date

-

Listing / Certification

2026-12-31

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Product Type Breakdown
28 total
  • BULK INGREDIENT
  • 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).

Visit FDA NDC Directory
Record Details Preview

Click "View Details" on any record above to expand full details inline.

Substance

CLOPIDOGREL BISULFATE

Identifiers

NDC: 60505-3992
DEA Schedule:

Official FDA Data

Based on publicly available FDA NDC information

National Drug Code

Structured NDC product information

Product Information

Drug, labeler and marketing data

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