Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Ltd
02 1Deccan Nutraceuticals Pvt. Ltd.
03 4C-squared PHARMA S.à r.l.
04 1LAURUS LABS LIMITED
05 2NOBILUS ENT TOMASZ KOZLUK
06 1Nobilus Ent Tomasz Kozluk
07 1Professional Compounding Centers of America
01 2DIGOXIN
02 8Digoxin
03 1Digoxin (Micron 10)
01 3India
02 4Ireland
03 3Poland
04 1United Kingdom
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC Package Code : 55742-123
Start Marketing Date : 2011-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Deccan Nutraceuticals: A global leader in the integrated development, manufacturing, and marketing of pharmaceutical products.
NDC Package Code : 45085-0101
Start Marketing Date : 2017-11-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69205-202
Start Marketing Date : 2020-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69205-101
Start Marketing Date : 2019-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69205-201
Start Marketing Date : 2020-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42385-101
Start Marketing Date : 2019-04-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59695-0001
Start Marketing Date : 2011-05-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59695-0002
Start Marketing Date : 2011-05-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59695-0004
Start Marketing Date : 2020-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0291
Start Marketing Date : 2018-12-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Lanoxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lanoxin, including repackagers and relabelers. The FDA regulates Lanoxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lanoxin 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 Lanoxin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lanoxin supplier is an individual or a company that provides Lanoxin active pharmaceutical ingredient (API) or Lanoxin finished formulations upon request. The Lanoxin suppliers may include Lanoxin API manufacturers, exporters, distributors and traders.
click here to find a list of Lanoxin 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 Lanoxin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lanoxin 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 Lanoxin 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 Lanoxin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lanoxin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lanoxin suppliers with NDC on PharmaCompass.
We have 6 companies offering Lanoxin
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