01 Hubei Gedian Humanwell Pharmaceutical (1)
02 Symbiotec Pharmalab (1)
03 3M Drug Delivery Systems (1)
04 Bayer AG (4)
05 Cipla (1)
06 FORTEQ NIDAU AG (1)
07 Formosa Laboratories (1)
08 Gedeon Richter (3)
09 Hunan KYX Pharmaceutical (1)
10 Indo Phyto Chemicals Private Ltd (1)
11 Industriale Chimica s.r.l. (1)
12 Lupin Ltd (2)
13 Qinhuangdao Zizhu Pharmaceutical Co., Ltd. (1)
14 ScinoPharm Taiwan, Ltd (2)
15 Sterling Spa (1)
16 Yangzhou Pharmaceutical Factory (1)
17 Blank (5)
01 CLIMARA PRO(R) ESTRADIOL/LEVONORGESTREL TRANSDERMAL DELIVERY SYSTEM (1)
02 LEVONORGESTREL (6)
03 LEVONORGESTREL (DCM) (1)
04 LEVONORGESTREL (MICRONIZED) (1)
05 LEVONORGESTREL EP/USP, MICRONIZED (1)
06 LEVONORGESTREL INTRAUTERINE DEVICE (1)
07 LEVONORGESTREL MICROCAPSULES (2)
08 LEVONORGESTREL USP (5)
09 LEVONORGESTREL USP 23 (1)
10 LEVONORGESTREL, USP (2)
11 MIRENA® INSERTER PROJECT (1)
12 NORGESTREL (1)
13 NORGESTREL USP (4)
14 NORPLANT (LEVONORGESTREL IMPLANTS) (1)
01 China (4)
02 Germany (4)
03 Hungary (3)
04 India (5)
05 Italy (2)
06 Switzerland (1)
07 Taiwan (3)
08 U.S.A (1)
09 Blank (5)
01 Active (18)
02 Inactive (10)
01 Complete (8)
02 Blank (20)
61
PharmaCompass offers a list of Levonorgestrel 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 Levonorgestrel manufacturer or Levonorgestrel supplier for your needs.
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PharmaCompass also assists you with knowing the Levonorgestrel API Price utilized in the formulation of products. Levonorgestrel API Price is not always fixed or binding as the Levonorgestrel Price is obtained through a variety of data sources. The Levonorgestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202872 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202872, including repackagers and relabelers. The FDA regulates Tox21_202872 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202872 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tox21_202872 supplier is an individual or a company that provides Tox21_202872 active pharmaceutical ingredient (API) or Tox21_202872 finished formulations upon request. The Tox21_202872 suppliers may include Tox21_202872 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_202872 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_202872 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202872 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202872 DMFs exist exist since differing nations have different regulations, such as Tox21_202872 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202872 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202872 USDMF includes data on Tox21_202872's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202872 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 16 companies offering Tox21_202872
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