01 1Catalent Micron Technologies, Inc.
02 1Excella GmbH & Co. KG
03 1Fagron Inc
04 1Fagron Services BV
05 1HETERO LABS LIMITED
06 1Hetero Drugs Limited
07 1Hubei Yitai Pharmaceutical Co., Ltd
08 1KALCHEM INTERNATIONAL INC
09 1LETCO MEDICAL, LLC
10 1MYLAN LABORATORIES LIMITED
11 1Medisca Inc.
12 1Olon S.p.A.
13 2Olon SpA
14 1PROFESSIONAL COMPOUNDING CENTERS OF AMERICA
15 1Piramal Pharma Limited
16 1Professional Compounding Centers of America
17 1Professional Compounding Centers of America dba PCCA
18 2Quimica Sintetica S.A.
19 2RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA
20 1Spectrum Laboratory Products, Inc.
21 1Tianish Laboratories Private Limited
22 1Union Quimico Farmaceutica SA (UQUIFA)-Sant Celoni
23 1YUNG ZIP CHEMICAL INDUSTRIAL CO., LTD.
24 1Zhejiang Charioteer Pharmaceutical Co, Ltd.
01 8ACYCLOVIR
02 17Acyclovir
03 1Acyclovir F
04 1Acyclovir Micronized
01 2China
02 3India
03 5Italy
04 1Luxembourg
05 2Netherlands
06 3Spain
07 1Taiwan
08 7U.S.A
09 3United Kingdom
NDC Package Code : 51552-0671
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-05-15
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 46014-1017
Start Marketing Date : 1994-09-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0173
Start Marketing Date : 2014-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0005
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0041
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0077
Start Marketing Date : 2017-05-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12711-9744
Start Marketing Date : 2007-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 12711-9755
Start Marketing Date : 1993-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 49452-0001
Start Marketing Date : 2000-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49711-0094
Start Marketing Date : 2009-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Aciclovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aciclovir, including repackagers and relabelers. The FDA regulates Aciclovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aciclovir 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 Aciclovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aciclovir supplier is an individual or a company that provides Aciclovir active pharmaceutical ingredient (API) or Aciclovir finished formulations upon request. The Aciclovir suppliers may include Aciclovir API manufacturers, exporters, distributors and traders.
click here to find a list of Aciclovir 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 Aciclovir as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aciclovir 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 Aciclovir 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 Aciclovir and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aciclovir NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aciclovir suppliers with NDC on PharmaCompass.
We have 19 companies offering Aciclovir
Get in contact with the supplier of your choice:
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