01 1Albemarle Corporation
02 1Glenmark Life Sciences Limited
03 1HOSTER LABS PRIVATE LIMITED
04 1LIVENT USA CORP.
05 1Novartis Pharmaceuticals Corporation
01 3Lithium Carbonate
02 1Lithium carbonate
03 1lithium carbonate
01 1India
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 : 2024-12-31
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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A Lithium Carbonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lithium Carbonate, including repackagers and relabelers. The FDA regulates Lithium Carbonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lithium Carbonate 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 Lithium Carbonate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lithium Carbonate supplier is an individual or a company that provides Lithium Carbonate active pharmaceutical ingredient (API) or Lithium Carbonate finished formulations upon request. The Lithium Carbonate suppliers may include Lithium Carbonate API manufacturers, exporters, distributors and traders.
click here to find a list of Lithium Carbonate 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 Lithium Carbonate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lithium Carbonate 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 Lithium Carbonate 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 Lithium Carbonate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lithium Carbonate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lithium Carbonate suppliers with NDC on PharmaCompass.
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