Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Catalana SL
02 1Supriya Lifescience Limited
03 1AX Pharmaceutical Corp
04 1Apex Healthcare Limited
05 1Asclemed USA Inc.
06 1Asclemed USA, Inc.
07 1B&B Pharmaceuticals, Inc.
08 1Cambrex Karlskoga AB
09 1Delta Synthetic Co. Ltd
10 1Fagron Inc
11 1Galenova Inc
12 1HETERO LABS LIMITED
13 1Harman Finochem Limited
14 1Isomedix Operations, Inc
15 1Kalchem International inc
16 1LETCO MEDICAL, LLC
17 1Medisca Inc.
18 1PROFESSIONAL COMPOUNDING CENTERS OF AMERICA
19 2Professional Compounding Centers of America
20 1Societa Italiana Medicinali Scandicci S.I.M.S., SrL
21 2Spectrum Laboratory Products, Inc.
22 2Swati Spentose Private Limited
23 1Unilab Chemicals and Pharmaceuticals Private Limited
24 2Village Pharma LLC
25 1W. R. GRACE & CO.-CONN.
26 1Xenex Laboratories Inc
01 2LIDOCAINE
02 1LIDOCAINE HCL
03 1LIDOCAINE HCL MONOHYDRATE
04 4LIDOCAINE HYDROCHLORIDE
05 2Lidocaine
06 1Lidocaine HCL
07 3Lidocaine HCl
08 14Lidocaine Hydrochloride
09 1Lidocaine hydrochloride
10 1lidocaine hydrochloride monohydrate
01 3Canada
02 7India
03 1Italy
04 2Latvia
05 1Netherlands
06 1Spain
07 1Taiwan
08 11U.S.A
09 3United Kingdom
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0701
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-2000
Start Marketing Date : 2011-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12651-113
Start Marketing Date : 2006-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0106
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 22568-1082
Start Marketing Date : 2006-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0082
Start Marketing Date : 2012-02-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12660-0321
Start Marketing Date : 1979-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4050
Start Marketing Date : 1998-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4051
Start Marketing Date : 2022-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 25119-5000
Start Marketing Date : 2021-05-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Lidocaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lidocaine Hydrochloride, including repackagers and relabelers. The FDA regulates Lidocaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lidocaine Hydrochloride 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 Lidocaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lidocaine Hydrochloride supplier is an individual or a company that provides Lidocaine Hydrochloride active pharmaceutical ingredient (API) or Lidocaine Hydrochloride finished formulations upon request. The Lidocaine Hydrochloride suppliers may include Lidocaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Lidocaine Hydrochloride 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 Lidocaine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lidocaine Hydrochloride 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 Lidocaine Hydrochloride 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 Lidocaine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lidocaine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lidocaine Hydrochloride suppliers with NDC on PharmaCompass.
We have 24 companies offering Lidocaine Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
