With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Teva API India Private Ltd
03 1Cambrex Profarmaco Milano Srl
04 2Chemeca Drugs Private Limited
05 1Divi's Laboratories Limited
06 1F.I.S. Fabbrica Italiana Sintetici S.P.A.
07 1Fagron Inc
08 2Galenova Inc
09 1HETERO LABS LIMITED
10 1Kalchem International inc
11 1LETCO MEDICAL, LLC
12 1Medisca Inc.
13 1Piramal Pharma Limited
14 1Spectrum Laboratory Products, Inc.
15 1Xenex Laboratories Inc
01 1DILTIAZEM
02 4DILTIAZEM HYDROCHLORIDE
03 1Diltiazem HCl
04 10Diltiazem Hydrochloride
05 1diltiazem hydrochloride
01 3Canada
02 1Finland
03 4India
04 1Israel
05 1Italy
06 1Netherlands
07 6U.S.A
With Fermion, start the journey of your innovative API.
NDC Package Code : 12780-2960
Start Marketing Date : 1985-02-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TAPI offers customized CDMO Solutions for API development and manufacturing services.
NDC Package Code : 15894-0022
Start Marketing Date : 2011-08-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0037
Start Marketing Date : 1986-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62331-005
Start Marketing Date : 1997-10-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52133-0013
Start Marketing Date : 1992-08-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0740
Start Marketing Date : 1998-04-01
End Marketing Date : 2027-02-03
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 60592-902
Start Marketing Date : 2022-04-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1046
Start Marketing Date : 2009-05-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0227
Start Marketing Date : 2014-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4881
Start Marketing Date : 1997-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Diltiazem Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diltiazem Hydrochloride, including repackagers and relabelers. The FDA regulates Diltiazem Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diltiazem Hydrochloride 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 Diltiazem Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diltiazem Hydrochloride supplier is an individual or a company that provides Diltiazem Hydrochloride active pharmaceutical ingredient (API) or Diltiazem Hydrochloride finished formulations upon request. The Diltiazem Hydrochloride suppliers may include Diltiazem Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Diltiazem Hydrochloride 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 Diltiazem Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diltiazem Hydrochloride 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 Diltiazem Hydrochloride 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 Diltiazem Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diltiazem Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diltiazem Hydrochloride suppliers with NDC on PharmaCompass.
We have 15 companies offering Diltiazem Hydrochloride
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