IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 1IOL Chemicals and Pharmaceuticals Ltd.
02 1Dr.Reddy's Laboratories Limited
03 1Neuland Laboratories Limited
04 1AMERICAN PACIFIC CORPORATION
05 1AX Pharmaceutical Corp
06 1Aurobindo Pharma Limited
07 1Darmerica, LLC
08 1Divi's Laboratories Limited
09 1EMNAR PHARMA PRIVATE LIMITED
10 1Esteve Quimica, SA
11 1Fagron Inc
12 2Hetero Labs Limited
13 1Honour Lab Limited
14 1Jubilant Pharmova Limited
15 1LETCO MEDICAL, LLC
16 1MSN Life Sciences Private Limited
17 1Medisca Inc.
18 1Professional Compounding Centers of America
19 1Professional Compounding Centers of America dba PCCA
20 1Rui Laboratories private limited
21 1SMS Pharmaceuticals Limited
22 1Shaoxing Jingxin Pharmaceutical Co., Ltd.
23 1Solara Active Pharma Sciences Limited
24 1Srini Pharmaceuticals Private Limited
25 1UCB Farchim S.A.
26 1UCB Pharma S.A.
27 1Venkata Narayana Active Ingredients Private Limited
28 1Wanbury Limited
29 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
30 1Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
31 1Zhejiang Huahai Pharmaceutical Co., Ltd.
01 8LEVETIRACETAM
02 21Levetiracetam
03 1Levetiracetam (Form-I)
04 2levetiracetam
01 1Belgium
02 1Canada
03 4China
04 17India
05 1Netherlands
06 1Spain
07 1Switzerland
08 4U.S.A
09 2United Kingdom
NDC Package Code : 49716-332
Start Marketing Date : 2023-10-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-870
Start Marketing Date : 2003-11-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58032-0132
Start Marketing Date : 2020-03-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50683-0322
Start Marketing Date : 2001-03-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1448
Start Marketing Date : 2012-01-02
End Marketing Date : 2025-09-30
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-2900
Start Marketing Date : 2017-05-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0088
Start Marketing Date : 2020-02-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 28877-0117
Start Marketing Date : 2000-04-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 36998-0117
Start Marketing Date : 2000-04-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12666-0014
Start Marketing Date : 2010-11-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Levetiracetam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levetiracetam, including repackagers and relabelers. The FDA regulates Levetiracetam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levetiracetam 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 Levetiracetam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levetiracetam supplier is an individual or a company that provides Levetiracetam active pharmaceutical ingredient (API) or Levetiracetam finished formulations upon request. The Levetiracetam suppliers may include Levetiracetam API manufacturers, exporters, distributors and traders.
click here to find a list of Levetiracetam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Levetiracetam as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Levetiracetam API and other APIs are published in this directory by the FDA.
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 Levetiracetam 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.
The NDC directory also contains data on finished compounded human drug products that contain Levetiracetam and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Levetiracetam NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Levetiracetam suppliers with NDC on PharmaCompass.
We have 29 companies offering Levetiracetam
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?