01 1APICORE PHARMACEUTICALS PRIVATE LIMITED
02 1Apothecon Pharmaceuticals Pvt Ltd
03 1Aurobindo Pharma Limited
04 1DARMERICA, LLC
05 2FLEMING LABORATORIES LIMITED
06 1Fagron Inc
07 1Fagron Services BV
08 1LETCO MEDICAL, LLC
09 1MSN Life Sciences Private Limited
10 1Optimus Drugs Private Limited
11 1Sionc Pharmaceutical Private Limited
12 1Suven Pharmaceuticals Limited
13 1Vijayasri Organics Private Limited
14 1sanPharmacy Inc.
01 3D-PENICILLAMINE
02 3PENICILLAMINE
03 8Penicillamine
04 1Penicillium frequentans (Penicillium glabrum)
01 10India
02 2Netherlands
03 2U.S.A
04 1Blank
NDC Package Code : 42973-230
Start Marketing Date : 2016-07-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-245
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-491
Start Marketing Date : 2021-11-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1096
Start Marketing Date : 2004-09-01
End Marketing Date : 2025-03-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-3190
Start Marketing Date : 2023-12-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 72640-012
Start Marketing Date : 2019-12-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-014
Start Marketing Date : 2017-10-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68022-7041
Start Marketing Date : 2016-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 70159-004
Start Marketing Date : 2017-09-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73479-131
Start Marketing Date : 2023-11-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (22)
Marketing Category : BULK INGREDIENT
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A Penicillamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penicillamine, including repackagers and relabelers. The FDA regulates Penicillamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penicillamine 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 Penicillamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Penicillamine supplier is an individual or a company that provides Penicillamine active pharmaceutical ingredient (API) or Penicillamine finished formulations upon request. The Penicillamine suppliers may include Penicillamine API manufacturers, exporters, distributors and traders.
click here to find a list of Penicillamine 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 Penicillamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Penicillamine 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 Penicillamine 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 Penicillamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Penicillamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Penicillamine suppliers with NDC on PharmaCompass.
We have 12 companies offering Penicillamine
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