Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Ltd
02 1NURAY CHEMICALS PRIVATE LIMITED
03 1Amphastar Nanjing Pharmaceuticals, Inc.
04 1Boehringer Ingelheim Pharma GmbH and Co. KG
05 2C-squared Pharma Sarl
06 1Fagron Inc
07 1Fagron Services BV
08 1Hubei Biocause Heilen Pharmaceutical Co., Ltd
09 1KALINTIS HEALTHCARE PRIVATE LIMITED
10 1Kalchem International inc
11 1LETCO MEDICAL, LLC
12 1Laurus Labs Limited
13 1MEDISCA Inc..
14 1MINSHENG GROUP SHAOXING PHARMACEUTICAL CO,. LTD.
15 1Professional Compounding Centers of America dba PCCA
16 1Rolabo Outsourcing, S.L.
17 1Saurav Chemicals Limited
18 1SpecGx LLC
01 1ATROPINE
02 4ATROPINE SULFATE
03 1ATROPINE SULFATE MONOHYDRATE
04 8Atropine Sulfate
05 1Atropine Sulphate monohydrate
06 1Atropine sulfate
07 1DIPHENOXYLATE HYDROCHLORIDE and ATROPINE SULFATE
08 1atropine sulfate
09 1diphenoxylate hydrochloride
01 2China
02 1Germany
03 5India
04 3Ireland
05 2Netherlands
06 1Spain
07 4U.S.A
08 1United Kingdom
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC Package Code : 55742-124
Start Marketing Date : 2014-09-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-059
Start Marketing Date : 2024-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12714-031
Start Marketing Date : 2001-07-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1391
Start Marketing Date : 2016-01-28
End Marketing Date : 2025-06-06
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 42385-736
Start Marketing Date : 2017-06-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
NDC Package Code : 0406-1593
Start Marketing Date : 2013-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (.01kg/kg .99kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 38779-2267
Start Marketing Date : 2018-12-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13371-387
Start Marketing Date : 2010-08-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1001
Start Marketing Date : 2013-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 43235-0004
Start Marketing Date : 2017-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Atropine Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atropine Sulfate, including repackagers and relabelers. The FDA regulates Atropine Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atropine Sulfate 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 Atropine Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atropine Sulfate supplier is an individual or a company that provides Atropine Sulfate active pharmaceutical ingredient (API) or Atropine Sulfate finished formulations upon request. The Atropine Sulfate suppliers may include Atropine Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Atropine Sulfate 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 Atropine Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Atropine Sulfate 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 Atropine Sulfate 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 Atropine Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Atropine Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Atropine Sulfate suppliers with NDC on PharmaCompass.
We have 17 companies offering Atropine Sulfate
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