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01 1Metrochem API Private Limited

02 2Dr.Reddy's Laboratories Limited

03 1Dr.Reddys Laboratories Limited

04 1Granules India Ltd

05 1Aurobindo Pharma Limited

06 1Chromo Laboratories India Private Limited

07 2Cipla Ltd.

08 1DISHMAN CARBOGEN AMCIS LIMITED

09 1EVEREST ORGANICS LIMITED

10 1Fagron Inc

11 1Glenmark Life Sciences Limited

12 1HETERO DRUGS LIMITED

13 1Hetero Drugs Limited

14 1Kalchem International inc

15 1LETCO MEDICAL, LLC

16 1MEDISCA Inc.

17 1Medisca Inc

18 1Medisca Inc.

19 1Natco Pharma Limited

20 1Professional Compounding Centers of America dba PCCA

21 2Quimica Sintetica S.A.

22 1ScinoPharm Taiwan Ltd.

23 1Shouguang Fukang Pharmaceutical Co., Ltd.

24 1Smilax Laboratories Limited

25 1Spectrum Laboratory Products, Inc.

26 1Srini Pharmaceuticals Private Limited

27 1TAPI Croatia Industries Ltd.

28 1Uquifa Spain

29 1Xenex Laboratories Inc

30 1Yung Shin Pharmaceutical Ind. Co., Ltd.

31 1Zhejiang Jinhua Conba Bio-Pharm. Co., LTD.

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PharmaCompass

01

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMetrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

OMEPRAZOLE

NDC Package Code : 42765-010

Start Marketing Date : 2020-06-22

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

Metrochem

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

OMEPRAZOLE

NDC Package Code : 55111-006

Start Marketing Date : 1998-03-25

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

03

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

OMEPRAZOLE

NDC Package Code : 62207-983

Start Marketing Date : 2023-01-09

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (20kg/20kg)

Marketing Category : BULK INGREDIENT

Granules India

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

OMEPRAZOLE

NDC Package Code : 55111-873

Start Marketing Date : 2006-08-28

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

OMEPRAZOLE

NDC Package Code : 55111-981

Start Marketing Date : 2015-09-16

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

06

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

OMEPRAZOLE

NDC Package Code : 38779-3183

Start Marketing Date : 2019-04-12

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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07

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

OMEPRAZOLE

NDC Package Code : 38779-3293

Start Marketing Date : 2023-05-24

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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08

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

OMEPRAZOLE

NDC Package Code : 38779-1935

Start Marketing Date : 2015-07-06

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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09

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

OMEPRAZOLE

NDC Package Code : 49452-4891

Start Marketing Date : 2001-12-01

End Marketing Date : 2025-07-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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10

TAPI Croatia Industries Ltd.

Country
PharmaVenue
Not Confirmed
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TAPI Croatia Industries Ltd.

Country
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PharmaVenue
Not Confirmed

OMEPRAZOLE

NDC Package Code : 11722-053

Start Marketing Date : 2022-12-13

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

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Omeprazole Manufacturers

A Omeprazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Omeprazole, including repackagers and relabelers. The FDA regulates Omeprazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Omeprazole API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Omeprazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Omeprazole Suppliers

A Omeprazole supplier is an individual or a company that provides Omeprazole active pharmaceutical ingredient (API) or Omeprazole finished formulations upon request. The Omeprazole suppliers may include Omeprazole API manufacturers, exporters, distributors and traders.

click here to find a list of Omeprazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Omeprazole NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Omeprazole as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Omeprazole API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Omeprazole as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Omeprazole and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Omeprazole NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Omeprazole suppliers with NDC on PharmaCompass.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.