01 1AX Pharmaceutical Corp
02 1Arene Life Sciences Private Limited
03 1Changzhou Tianhua Pharmaceutical Co., Ltd.
04 1DARMERICA, LLC
05 2Fagron Inc
06 1Fagron Services BV
07 1Flamma S.p.A.
08 1GLOBAL CALCIUM PRIVATE LIMITED
09 1Galenova Inc
10 1Icrom S.r.l.
11 1KALCHEM INTERNATIONAL INC
12 1Kumar Organic Products Limited
13 2LETCO MEDICAL, LLC
14 1Medisca Inc.
15 1OLON ACTIVE PHARMACEUTICAL INGREDIENTS INDIA PRIVATE LIMITED
16 1Olon SpA
17 1Pharma Source Direct, Inc.
18 2Pharmacia and Upjohn Company LLC
19 1Professional Compounding Centers of America
20 1Professional Compounding Centers of America dba PCCA
21 1SMS Lifesciences India Limited
22 1Spectrum Laboratory Products, Inc.
23 1Symbio Generrics India Private Limited
24 1Trifarma S.p.A
25 1Willow Birch Pharma, Inc
26 1Willow Birch Pharma, Inc.
27 1Xenex Laboratories Inc
01 8MINOXIDIL
02 1MINOXIDIL MICRONIZED
03 21Minoxidil
01 3Canada
02 1China
03 4India
04 5Italy
05 3Netherlands
06 11U.S.A
07 2United Kingdom
08 1Blank
NDC Package Code : 51552-0536
Start Marketing Date : 2004-09-01
End Marketing Date : 2026-02-28
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 40700-0008
Start Marketing Date : 2020-02-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0574
Start Marketing Date : 2008-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17337-0027
Start Marketing Date : 1988-05-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0009-5056
Start Marketing Date : 2020-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0009-5230
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 : 49452-4780
Start Marketing Date : 1996-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46204-0159
Start Marketing Date : 2017-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-149
Start Marketing Date : 2024-05-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-149
Start Marketing Date : 2023-06-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Minoxidil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minoxidil, including repackagers and relabelers. The FDA regulates Minoxidil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minoxidil 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 Minoxidil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Minoxidil supplier is an individual or a company that provides Minoxidil active pharmaceutical ingredient (API) or Minoxidil finished formulations upon request. The Minoxidil suppliers may include Minoxidil API manufacturers, exporters, distributors and traders.
click here to find a list of Minoxidil 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 Minoxidil as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Minoxidil 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 Minoxidil 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 Minoxidil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Minoxidil NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Minoxidil suppliers with NDC on PharmaCompass.
We have 22 companies offering Minoxidil
Get in contact with the supplier of your choice:
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