01 1Dipharma Francis Srl
02 1LETCO MEDICAL, LLC
03 1Medisca Inc.
04 1Olon S.p.A.
05 1Olon SpA
06 1R.L.Fine Chem Private Limited
07 1Spectrum Laboratory Products, Inc.
08 2Vasudha Pharma Chem Limited
01 2CYPROHEPTADINE HYDROCHLORIDE
02 6Cyproheptadine Hydrochloride
03 1Cyproheptadine hydrochloride
01 3India
02 3Italy
03 3U.S.A
NDC Package Code : 46438-0036
Start Marketing Date : 1980-01-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1232
Start Marketing Date : 2011-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-1226
Start Marketing Date : 2014-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0508
Start Marketing Date : 2017-04-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0553
Start Marketing Date : 2024-09-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71554-003
Start Marketing Date : 2019-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-2409
Start Marketing Date : 2000-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66577-014
Start Marketing Date : 2018-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66577-040
Start Marketing Date : 2018-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Cyproheptadine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyproheptadine Hydrochloride, including repackagers and relabelers. The FDA regulates Cyproheptadine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyproheptadine 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 Cyproheptadine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyproheptadine Hydrochloride supplier is an individual or a company that provides Cyproheptadine Hydrochloride active pharmaceutical ingredient (API) or Cyproheptadine Hydrochloride finished formulations upon request. The Cyproheptadine Hydrochloride suppliers may include Cyproheptadine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cyproheptadine 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 Cyproheptadine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cyproheptadine 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 Cyproheptadine 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 Cyproheptadine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cyproheptadine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cyproheptadine Hydrochloride suppliers with NDC on PharmaCompass.
We have 7 companies offering Cyproheptadine Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
