01 1C-SQUARED PHARMA LIMITED
02 1Industriale Chimica s.r.l.
03 1Pharmacia and Upjohn Company LLC
04 3QINGDAO TIDA BIOTEK CO.,LTD
05 1Viatris Pharmaceuticals LLC
01 7Latanoprost
01 3China
02 1Ireland
03 1Italy
04 2U.S.A
NDC Package Code : 82133-103
Start Marketing Date : 2023-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0710
Start Marketing Date : 1996-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0009-5172
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 90027-006
Start Marketing Date : 2023-03-09
End Marketing Date : 2026-03-02
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 90027-006
Start Marketing Date : 2021-01-09
End Marketing Date : 2026-03-02
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 90027-031
Start Marketing Date : 2023-09-25
End Marketing Date : 2026-12-28
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 65427-007
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
11
PharmaCompass offers a list of Latanoprost 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 Latanoprost manufacturer or Latanoprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Latanoprost manufacturer or Latanoprost supplier.
PharmaCompass also assists you with knowing the Latanoprost API Price utilized in the formulation of products. Latanoprost API Price is not always fixed or binding as the Latanoprost Price is obtained through a variety of data sources. The Latanoprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iopize manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iopize, including repackagers and relabelers. The FDA regulates Iopize manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iopize 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 Iopize manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iopize supplier is an individual or a company that provides Iopize active pharmaceutical ingredient (API) or Iopize finished formulations upon request. The Iopize suppliers may include Iopize API manufacturers, exporters, distributors and traders.
click here to find a list of Iopize 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 Iopize as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Iopize 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 Iopize 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 Iopize and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Iopize NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Iopize suppliers with NDC on PharmaCompass.
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