01 1Edmond Pharma S.R.L
02 1Emcure Pharmaceuticals Limited
03 4Industriale Chimica s.r.l.
04 1Ipca Laboratories Limited
05 1Optimus Drugs Private Limited
06 2Sterling Pharma Solutions Limited
01 2MIDODRINE HYDROCHLORIDE
02 8Midodrine Hydrochloride
01 3India
02 4Italy
03 1Sweden
04 2United Kingdom
NDC Package Code : 14593-917
Start Marketing Date : 2021-07-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0580
Start Marketing Date : 1996-09-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0080
Start Marketing Date : 2004-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0720
Start Marketing Date : 1996-09-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0080
Start Marketing Date : 2004-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1204
Start Marketing Date : 2013-07-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-043
Start Marketing Date : 2021-12-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66583-0509
Start Marketing Date : 2005-09-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50384-0810
Start Marketing Date : 2003-03-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50384-0800
Start Marketing Date : 2003-03-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A ( -)-Midodrine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ( -)-Midodrine hydrochloride, including repackagers and relabelers. The FDA regulates ( -)-Midodrine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ( -)-Midodrine hydrochloride 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 ( -)-Midodrine hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ( -)-Midodrine hydrochloride supplier is an individual or a company that provides ( -)-Midodrine hydrochloride active pharmaceutical ingredient (API) or ( -)-Midodrine hydrochloride finished formulations upon request. The ( -)-Midodrine hydrochloride suppliers may include ( -)-Midodrine hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of ( -)-Midodrine hydrochloride 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 ( -)-Midodrine hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ( -)-Midodrine hydrochloride 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 ( -)-Midodrine hydrochloride 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 ( -)-Midodrine hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ( -)-Midodrine hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ( -)-Midodrine hydrochloride suppliers with NDC on PharmaCompass.
We have 6 companies offering ( -)-Midodrine hydrochloride
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