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01 1CENTRIENT PHARMACEUTICALS INDIA PRIVATE LIMITED

02 1Teva API India Private Limited

03 1Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)

04 1Arch Pharmalabs Limited

05 2Biocon Limited

06 1Cadila Pharmaceuticals Limited

07 1Changzhou Pharmaceutical Factory

08 1Chromo Laboratories India Private Limited

09 1Hetero Drugs Limited

10 1Hetero Labs Limited

11 1Jubilant Pharmova Limited

12 1MSN Life Sciences Private Limited

13 3MSN Pharmachem Private Limited

14 1MYLAN LABORATORIES LIMITED

15 1Novartis Pharmaceuticals Corporation

16 1PURE AND CURE HEALTHCARE PRIVATE LIMITED

17 1Professional Compounding Centers of America dba PCCA

18 2Tianish Laboratories Private Limited

19 1Upjohn Manufacturing Ireland Unlimited Company

20 1Willow Birch Pharma, Inc

21 1ZHEJIANG LEPU PHARMACEUTICAL CO., LTD.

22 1Zhejiang Jiangbei Pharmaceutical Co., Ltd.

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PharmaCompass

01

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCentrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.

ATORVASTATIN CALCIUM TRIHYDRATE

NDC Package Code : 70269-300

Start Marketing Date : 2015-08-20

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

Centrient Pharmaceuticals

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

ATORVASTATIN CALCIUM TRIHYDRATE

NDC Package Code : 15894-0023

Start Marketing Date : 2013-01-23

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

TAPI Company Banner

03

PharmaVenue
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08

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ATORVASTATIN CALCIUM TRIHYDRATE

NDC Package Code : 51927-5153

Start Marketing Date : 2021-09-21

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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09

PharmaVenue
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ATORVASTATIN CALCIUM TRIHYDRATE

NDC Package Code : 10695-166

Start Marketing Date : 2024-05-28

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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10

PharmaVenue
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ATORVASTATIN CALCIUM TRIHYDRATE

NDC Package Code : 13403-215

Start Marketing Date : 2024-09-30

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Atorvastatin Manufacturers

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

Atorvastatin Suppliers

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

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

Atorvastatin 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 Atorvastatin as an active pharmaceutical ingredient (API).

Finished drug products

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

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

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.