Veranova: A CDMO that manages complexity with confidence.
01 2Veranova, L.P.
02 1Noramco, LLC
03 1Purisys LLC
04 5B&B Pharmaceuticals, Inc.
05 1Cambrex Charles City, Inc
06 1Chattem Chemicals, Inc.
07 1Fagron Inc
08 1Janssen Pharmaceutical Sciences Unlimited
09 1LETCO MEDICAL, LLC
10 1Medisca Inc.
11 1Pharma Source Direct, Inc.
12 3Professional Compounding Centers of America
13 1Siegfried USA, LLC
14 2SpecGx LLC
15 1Spectrum Laboratory Products, Inc.
01 5HYDROMORPHONE HYDROCHLORIDE
02 3Hydromorphone HCL
03 5Hydromorphone HCl
04 10Hydromorphone Hydrochloride
01 2Ireland
02 1Netherlands
03 1Switzerland
04 16U.S.A
05 3United Kingdom
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0124
Start Marketing Date : 1995-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
NDC Package Code : 51634-0057
Start Marketing Date : 2006-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73548-0057
Start Marketing Date : 2021-07-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0141
Start Marketing Date : 1996-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0682
Start Marketing Date : 2004-09-01
End Marketing Date : 2027-03-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0406-3222
Start Marketing Date : 2011-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-3245
Start Marketing Date : 1981-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0731
Start Marketing Date : 2017-08-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0792-0632
Start Marketing Date : 2008-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-0029
Start Marketing Date : 1998-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Hydromorphone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydromorphone Hydrochloride, including repackagers and relabelers. The FDA regulates Hydromorphone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydromorphone 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 Hydromorphone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydromorphone Hydrochloride supplier is an individual or a company that provides Hydromorphone Hydrochloride active pharmaceutical ingredient (API) or Hydromorphone Hydrochloride finished formulations upon request. The Hydromorphone Hydrochloride suppliers may include Hydromorphone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Hydromorphone 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 Hydromorphone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydromorphone 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 Hydromorphone 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 Hydromorphone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydromorphone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydromorphone Hydrochloride suppliers with NDC on PharmaCompass.
We have 15 companies offering Hydromorphone Hydrochloride
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