Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 2ZAKLADY FARMACEUTYCZNE POLPHARMA S A
02 1Supriya Lifescience Limited
03 1AX Pharmaceutical Corp.
04 2Almon Healthcare Private Limited
05 1Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)
06 1Aurobindo Pharma Limited
07 1Azico Biophore India Private Limited
08 1B&B Pharmaceuticals, Inc.
09 1Cadila Pharmaceuticals Limited
10 1DARMERICA, LLC
11 1Fagron Inc
12 1Hetero Drugs Limited
13 1KALCHEM INTERNATIONAL INC
14 1LETCO MEDICAL, LLC
15 1MEDISCA Inc.
16 1MSN Organics Private Limited
17 1MYLAN LABORATORIES LIMITED
18 1Mylan Laboratories Limited
19 1Pharma Source Direct, Inc.
20 1Professional Compounding Centers of America dba PCCA
21 1Raks Pharma Pvt. Limited
22 1SMS Lifesciences India Limited
23 2SMS Pharmaceuticals Limited
24 1Spectrum Laboratory Products, Inc.
25 1Tianish Laboratories Private Limited
26 1Willow Birch Pharma, Inc.
27 1Xenex Laboratories Inc
01 1SILDENAFIL
02 10SILDENAFIL CITRATE
03 18Sildenafil Citrate
04 1sildenafil citrate
01 2Canada
02 12India
03 1Netherlands
04 2Poland
05 10U.S.A
06 1United Kingdom
07 2Blank
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0585
Start Marketing Date : 1998-03-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-1500
Start Marketing Date : 2014-04-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0586
Start Marketing Date : 1998-03-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (30kg/30kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1352
Start Marketing Date : 2004-09-01
End Marketing Date : 2027-05-29
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-2950
Start Marketing Date : 2017-03-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0001
Start Marketing Date : 2010-03-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5067
Start Marketing Date : 2019-08-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 47621-005
Start Marketing Date : 2018-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-7528
Start Marketing Date : 2016-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-017
Start Marketing Date : 2016-07-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Sildenafil Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sildenafil Citrate, including repackagers and relabelers. The FDA regulates Sildenafil Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sildenafil Citrate 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 Sildenafil Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sildenafil Citrate supplier is an individual or a company that provides Sildenafil Citrate active pharmaceutical ingredient (API) or Sildenafil Citrate finished formulations upon request. The Sildenafil Citrate suppliers may include Sildenafil Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sildenafil Citrate 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 Sildenafil Citrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sildenafil Citrate 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 Sildenafil Citrate 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 Sildenafil Citrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sildenafil Citrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sildenafil Citrate suppliers with NDC on PharmaCompass.
We have 25 companies offering Sildenafil Citrate
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