01 1Fine Chemicals Corporation (PTY) Ltd.
02 1Dr.Reddy's Laboratories Limited
03 1Apothecon Pharmaceuticals Pvt Ltd
04 1Curia Wisconsin, Inc.
05 1Harman Finochem Limited
06 1KALINTIS HEALTHCARE PRIVATE LIMITED
01 1BENZTROPINE MESYLATE
02 4Benztropine Mesylate
03 1benztropine mesylate
01 4India
02 1South Africa
03 1U.S.A
NDC Package Code : 48954-448
Start Marketing Date : 1987-04-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 30007-817
Start Marketing Date : 2010-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76339-138
Start Marketing Date : 2019-09-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (4.999kg/4.999kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64181-0088
Start Marketing Date : 1996-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66064-1023
Start Marketing Date : 2017-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72166-005
Start Marketing Date : 2018-04-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Benztropine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benztropine, including repackagers and relabelers. The FDA regulates Benztropine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benztropine 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 Benztropine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benztropine supplier is an individual or a company that provides Benztropine active pharmaceutical ingredient (API) or Benztropine finished formulations upon request. The Benztropine suppliers may include Benztropine API manufacturers, exporters, distributors and traders.
click here to find a list of Benztropine 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 Benztropine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Benztropine 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 Benztropine 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 Benztropine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Benztropine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Benztropine suppliers with NDC on PharmaCompass.
We have 6 companies offering Benztropine
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