Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1Noramco, LLC
03 1B&B Pharmaceuticals, Inc.
04 3Cambrex Charles City, Inc
05 1Chattem Chemicals, Inc.
06 1Fagron Inc
07 1LETCO MEDICAL, LLC
08 1Medisca Inc.
09 1Pharma Source Direct, Inc.
10 1Professional Compounding Centers of America
11 1Professional Compounding Centers of America dba PCCA
12 1Siegfried USA, LLC
13 3SpecGx LLC
14 1Spectrum Laboratory Products, Inc.
01 1Camouflage Hydrocodone
02 3HYDROCODONE BITARTRATE
03 1HYDROCODONE BITARTRATE HYDRATE
04 12Hydrocodone Bitartrate
05 1Hydrocodone Polistirex
01 3Ireland
02 1Netherlands
03 1Switzerland
04 11U.S.A
05 2United Kingdom
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0132
Start Marketing Date : 1996-01-01
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 : 51634-0014
Start Marketing Date : 1987-07-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0677
Start Marketing Date : 2004-09-01
End Marketing Date : 2025-08-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0406-8803
Start Marketing Date : 2013-12-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.56kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 0406-1559
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 : 0406-1582
Start Marketing Date : 1973-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0764
Start Marketing Date : 2014-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0048
Start Marketing Date : 1999-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0792-0543
Start Marketing Date : 2006-05-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-0033
Start Marketing Date : 1997-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Hydrocodone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocodone, including repackagers and relabelers. The FDA regulates Hydrocodone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocodone 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 Hydrocodone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocodone supplier is an individual or a company that provides Hydrocodone active pharmaceutical ingredient (API) or Hydrocodone finished formulations upon request. The Hydrocodone suppliers may include Hydrocodone API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocodone 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 Hydrocodone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydrocodone 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 Hydrocodone 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 Hydrocodone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydrocodone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydrocodone suppliers with NDC on PharmaCompass.
We have 13 companies offering Hydrocodone
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
