Axplora- The partner of choice for complex APIs.
01 1Farmabios S.p.A.
02 1Aspen Oss B.V.
03 1NURAY CHEMICALS PRIVATE LIMITED
04 1Symbiotec Pharmalab Private Limited
05 1ASG Biochem Pvt. LTD
06 1LETCO MEDICAL, LLC
07 1Professional Compounding Centers of America
08 1Professional Compounding Centers of America dba PCCA
09 1SHAKTI LIFESCIENCE PRIVATE LIMITED
01 3METHYLTESTOSTERONE
02 1METHYLTESTOSTERONEMICRONIZED
03 5Methyltestosterone
01 1Germany
02 4India
03 1Netherlands
04 1U.S.A
05 2United Kingdom
NDC Package Code : 46439-8741
Start Marketing Date : 2011-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60870-0232
Start Marketing Date : 1980-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-070
Start Marketing Date : 2024-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22552-0020
Start Marketing Date : 2010-05-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43647-345
Start Marketing Date : 1983-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-3177
Start Marketing Date : 2022-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0312
Start Marketing Date : 2023-08-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1028
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 73774-017
Start Marketing Date : 2023-10-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Methyltestosterone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyltestosterone, including repackagers and relabelers. The FDA regulates Methyltestosterone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyltestosterone 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 Methyltestosterone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methyltestosterone supplier is an individual or a company that provides Methyltestosterone active pharmaceutical ingredient (API) or Methyltestosterone finished formulations upon request. The Methyltestosterone suppliers may include Methyltestosterone API manufacturers, exporters, distributors and traders.
click here to find a list of Methyltestosterone 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 Methyltestosterone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methyltestosterone 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 Methyltestosterone 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 Methyltestosterone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methyltestosterone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methyltestosterone suppliers with NDC on PharmaCompass.
We have 8 companies offering Methyltestosterone
Get in contact with the supplier of your choice:
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