01 1Albemarle Corporation
02 1Glenmark Life Sciences Limited
03 1HOSTER LABS PRIVATE LIMITED
04 1LIVENT USA CORP.
05 1Novartis Pharmaceuticals Corporation
06 1Unique Chemicals
01 4Lithium Carbonate
02 1Lithium carbonate
03 1lithium carbonate
01 2India
02 1Switzerland
03 2U.S.A
04 1Blank
NDC Package Code : 39345-5104
Start Marketing Date : 2015-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-947
Start Marketing Date : 2018-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48589-0010
Start Marketing Date : 2025-02-03
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82388-001
Start Marketing Date : 2021-11-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0078-1378
Start Marketing Date : 2009-02-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82708-0008
Start Marketing Date : 1982-01-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Lithium Carbonate 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 Lithium Carbonate manufacturer or Lithium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lithium Carbonate manufacturer or Lithium Carbonate supplier.
PharmaCompass also assists you with knowing the Lithium Carbonate API Price utilized in the formulation of products. Lithium Carbonate API Price is not always fixed or binding as the Lithium Carbonate Price is obtained through a variety of data sources. The Lithium Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Quilonum retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quilonum retard, including repackagers and relabelers. The FDA regulates Quilonum retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quilonum retard 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 Quilonum retard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quilonum retard supplier is an individual or a company that provides Quilonum retard active pharmaceutical ingredient (API) or Quilonum retard finished formulations upon request. The Quilonum retard suppliers may include Quilonum retard API manufacturers, exporters, distributors and traders.
click here to find a list of Quilonum retard 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 Quilonum retard as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Quilonum retard 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 Quilonum retard 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 Quilonum retard and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Quilonum retard NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Quilonum retard suppliers with NDC on PharmaCompass.
We have 5 companies offering Quilonum retard
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