01 1Chemische Fabrik Berg GmbH
02 1Malladi Drugs & Pharmaceuticals Limited
03 1B&B Pharmaceuticals, Inc.
04 1Fagron Inc
05 1LETCO MEDICAL, LLC
06 1Medisca Inc.
07 1Olon SpA
08 1Professional Compounding Centers of America
09 1Professional Compounding Centers of America dba PCCA
10 2Siegfried USA, LLC
11 1Symed Labs Limited
01 1PHENTERMINE HYDROCHLORIDE
02 1Phentermine HCL
03 1Phentermine HCl
04 1Phentermine Hcl
05 7Phentermine Hydrochloride
06 1Phentermine hydrochloride
01 1Germany
02 2India
03 1Italy
04 1Netherlands
05 2Switzerland
06 3U.S.A
07 2United Kingdom
NDC Package Code : 65319-1452
Start Marketing Date : 2019-01-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-953
Start Marketing Date : 2024-11-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1354
Start Marketing Date : 2012-01-02
End Marketing Date : 2027-11-16
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-2681
Start Marketing Date : 2009-10-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0854
Start Marketing Date : 2006-02-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0030
Start Marketing Date : 2012-12-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0350
Start Marketing Date : 2024-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-2937
Start Marketing Date : 2013-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0792-0344
Start Marketing Date : 1979-01-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-0345
Start Marketing Date : 2015-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Ionamin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ionamin Hydrochloride, including repackagers and relabelers. The FDA regulates Ionamin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ionamin 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 Ionamin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ionamin Hydrochloride supplier is an individual or a company that provides Ionamin Hydrochloride active pharmaceutical ingredient (API) or Ionamin Hydrochloride finished formulations upon request. The Ionamin Hydrochloride suppliers may include Ionamin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ionamin 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 Ionamin Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ionamin 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 Ionamin 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 Ionamin Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ionamin Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ionamin Hydrochloride suppliers with NDC on PharmaCompass.
We have 10 companies offering Ionamin Hydrochloride
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