Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1Noramco Coventry LLC
03 2Noramco, LLC
04 2Catalent Micron Technologies, Inc.
05 1Chattem Chemicals, Inc.
06 1LETCO MEDICAL, LLC
07 1Medisca Inc.
08 1Pharma Source Direct, Inc.
09 1Professional Compounding Centers of America
10 1Professional Compounding Centers of America dba PCCA
11 1Siegfried USA, LLC
12 4SpecGx LLC
13 1Spectrum Laboratory Products, Inc.
01 1OXYCODONE BASE
02 1OXYCODONE HCL COARSE SIFTED
03 1OXYCODONE HCL LOW - ALPHA BETA UNSATURATED KETONE
04 2OXYCODONE HYDROCHLORIDE
05 1OXYCODONE HYDROCHLORIDE D
06 2Oxycodone HCl
07 1Oxycodone Hcl
08 7Oxycodone Hydrochloride
09 1Oxycodone base
10 1Purified Oxycodone Base
01 4Ireland
02 1Switzerland
03 11U.S.A
04 2United Kingdom
NDC Package Code : 49812-0150
Start Marketing Date : 2010-06-01
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 : 51634-0002
Start Marketing Date : 2000-01-01
End Marketing Date : 2025-12-31
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 : 51634-0003
Start Marketing Date : 2008-02-21
End Marketing Date : 2025-12-31
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 : 67509-006
Start Marketing Date : 2003-02-03
End Marketing Date : 2026-03-23
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-8853
Start Marketing Date : 2012-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-8865
Start Marketing Date : 1986-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-8873
Start Marketing Date : 2008-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-8180
Start Marketing Date : 2012-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0725
Start Marketing Date : 2014-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0792-2936
Start Marketing Date : 2010-02-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Oxycodone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxycodone Hydrochloride, including repackagers and relabelers. The FDA regulates Oxycodone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxycodone 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 Oxycodone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxycodone Hydrochloride supplier is an individual or a company that provides Oxycodone Hydrochloride active pharmaceutical ingredient (API) or Oxycodone Hydrochloride finished formulations upon request. The Oxycodone Hydrochloride suppliers may include Oxycodone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxycodone 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 Oxycodone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxycodone 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 Oxycodone 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 Oxycodone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxycodone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxycodone Hydrochloride suppliers with NDC on PharmaCompass.
We have 11 companies offering Oxycodone Hydrochloride
Get in contact with the supplier of your choice:
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