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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

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PharmaCompass

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMalladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.

PHENTERMINE HYDROCHLORIDE

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

Malladi

03

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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PHENTERMINE HYDROCHLORIDE

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...

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04

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

PHENTERMINE HYDROCHLORIDE

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

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05

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

PHENTERMINE HYDROCHLORIDE

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

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06

AACR Annual meeting
Not Confirmed
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07

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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PHENTERMINE HYDROCHLORIDE

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...

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08

AACR Annual meeting
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AACR Annual meeting
Not Confirmed

PHENTERMINE HYDROCHLORIDE

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...

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09

AACR Annual meeting
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PHENTERMINE HYDROCHLORIDE

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...

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10

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Looking for 1197-21-3 / Phentermine Hydrochloride API manufacturers, exporters & distributors?

Phentermine Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Phentermine Hydrochloride 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 Phentermine Hydrochloride manufacturer or Phentermine Hydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phentermine Hydrochloride manufacturer or Phentermine Hydrochloride supplier.

PharmaCompass also assists you with knowing the Phentermine Hydrochloride API Price utilized in the formulation of products. Phentermine Hydrochloride API Price is not always fixed or binding as the Phentermine Hydrochloride Price is obtained through a variety of data sources. The Phentermine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Phentermine Hydrochloride

Synonyms

1197-21-3, Phentermine hcl, Fastin, Oby-trim, Phenteral, Tora

Cas Number

1197-21-3

Unique Ingredient Identifier (UNII)

0K2I505OTV

About Phentermine Hydrochloride

A central nervous system stimulant and sympathomimetic with actions and uses similar to those of DEXTROAMPHETAMINE. It has been used most frequently in the treatment of obesity.

QSYMIA Manufacturers

A QSYMIA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QSYMIA, including repackagers and relabelers. The FDA regulates QSYMIA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QSYMIA 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 QSYMIA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

QSYMIA Suppliers

A QSYMIA supplier is an individual or a company that provides QSYMIA active pharmaceutical ingredient (API) or QSYMIA finished formulations upon request. The QSYMIA suppliers may include QSYMIA API manufacturers, exporters, distributors and traders.

click here to find a list of QSYMIA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

QSYMIA NDC

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 QSYMIA as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for QSYMIA API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 QSYMIA 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain QSYMIA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a QSYMIA NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of QSYMIA suppliers with NDC on PharmaCompass.

QSYMIA Manufacturers | Traders | Suppliers

QSYMIA Manufacturers, Traders, Suppliers 1
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Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.