SWATI - Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
01 3Swati Spentose Private Limited
02 1Moehs Catalana SL
03 1Apex Healthcare Limited
04 1AX Pharmaceutical Corp
05 1Cambrex Karlskoga AB
06 1DARMERICA, LLC
07 1Delta Synthetic Co. Ltd
08 1Fagron Inc
09 1Harman Finochem Limited
10 1KALCHEM INTERNATIONAL INC
11 1LARKSPUR ENTERPRISES LLC
12 1LETCO MEDICAL, LLC
13 2Medisca Inc.
14 1PROFESSIONAL COMPOUNDING CENTERS OF AMERICA
15 1Professional Compounding Centers of America
16 1Societa Italiana Medicinali Scandicci S.I.M.S., SrL
17 1Spectrum Laboratory Products, Inc.
18 1W. R. GRACE & CO.-CONN.
19 1Xenex Laboratories Inc
20 1Zen Chemicals Private Limited
01 5LIDOCAINE
02 1LIDOCAINE BASE
03 17Lidocaine
01 2Canada
02 5India
03 1Italy
04 1Japan
05 1Netherlands
06 1Spain
07 1Taiwan
08 8U.S.A
09 2United Kingdom
10 1Blank
SWATI - Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
NDC Package Code : 52119-001
Start Marketing Date : 2012-08-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0702
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
NDC Package Code : 69617-009
Start Marketing Date : 2019-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
SWATI - Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
NDC Package Code : 52119-008
Start Marketing Date : 2014-03-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SWATI - Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
NDC Package Code : 52119-019
Start Marketing Date : 2019-08-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12651-124
Start Marketing Date : 2023-10-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1014
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0081
Start Marketing Date : 2012-04-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-3333
Start Marketing Date : 2025-09-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12660-0033
Start Marketing Date : 1989-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Lidocaine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Lidocaine manufacturer or Lidocaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lidocaine manufacturer or Lidocaine supplier.
PharmaCompass also assists you with knowing the Lidocaine API Price utilized in the formulation of products. Lidocaine API Price is not always fixed or binding as the Lidocaine Price is obtained through a variety of data sources. The Lidocaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LIDODERM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIDODERM, including repackagers and relabelers. The FDA regulates LIDODERM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIDODERM 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 LIDODERM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LIDODERM supplier is an individual or a company that provides LIDODERM active pharmaceutical ingredient (API) or LIDODERM finished formulations upon request. The LIDODERM suppliers may include LIDODERM API manufacturers, exporters, distributors and traders.
click here to find a list of LIDODERM 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 LIDODERM as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for LIDODERM 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 LIDODERM 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 LIDODERM and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a LIDODERM NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of LIDODERM suppliers with NDC on PharmaCompass.
We have 18 companies offering LIDODERM
Get in contact with the supplier of your choice:
