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01 1CIPAN-Companhia Industrial Produtora de Antibióticos, S.A.

02 1AX Pharmaceutical Corp

03 1FUJIAN FUKANG PHARMACEUTICAL CO., LTD.

04 1Fagron Inc

05 1LETCO MEDICAL, LLC

06 1Medisca Inc.

07 1Ningxia Qiyuan Pharmaceutical Co., Ltd.

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSuanfarma, at the Core of a Better Life.

TETRACYCLINE HYDROCHLORIDE

NDC Package Code : 17158-0100

Start Marketing Date : 2017-12-17

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Suanfarma

02

BIO CEO & Investor
Not Confirmed
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BIO CEO & Investor
Not Confirmed

TETRACYCLINE HYDROCHLORIDE

NDC Package Code : 73377-301

Start Marketing Date : 2024-11-08

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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03

BIO CEO & Investor
Not Confirmed
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BIO CEO & Investor
Not Confirmed

TETRACYCLINE HYDROCHLORIDE

NDC Package Code : 51552-0463

Start Marketing Date : 2004-09-01

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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04

BIO CEO & Investor
Not Confirmed
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BIO CEO & Investor
Not Confirmed

TETRACYCLINE HYDROCHLORIDE

NDC Package Code : 67630-0007

Start Marketing Date : 2018-09-07

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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05

BIO CEO & Investor
Not Confirmed
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BIO CEO & Investor
Not Confirmed

TETRACYCLINE HYDROCHLORIDE

NDC Package Code : 62991-2941

Start Marketing Date : 2010-09-16

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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06

BIO CEO & Investor
Not Confirmed
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BIO CEO & Investor
Not Confirmed

TETRACYCLINE HYDROCHLORIDE

NDC Package Code : 38779-0053

Start Marketing Date : 2012-02-28

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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07

BIO CEO & Investor
Not Confirmed
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BIO CEO & Investor
Not Confirmed

TETRACYCLINE HYDROCHLORIDE

NDC Package Code : 59566-0350

Start Marketing Date : 2004-10-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Actisite Manufacturers

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

Actisite Suppliers

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

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

Actisite 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 Actisite as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Actisite 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 Actisite 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 Actisite and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Actisite NDC to their finished compounded human drug products, they may choose to do so.

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

Actisite Manufacturers | Traders | Suppliers

Actisite Manufacturers, Traders, Suppliers 1
35

We have 7 companies offering Actisite

Get in contact with the supplier of your choice:

  1. Suanfarma
  2. Ax Pharmaceutical Corporation
  3. Fagron Group
  4. FUJIAN FUKANG PHARMACEUTICAL
  5. Letco Medical
  6. Medisca
  7. Ningxia Qiyuan Pharmaceutical
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.