Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022272

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OXYCONTIN (OXYCODONE HYDROCHLORIDE)
10MG Marketing Status: Prescription

Active Ingredient: OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 10MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N022272
Product Number: 001
Approval Date: Apr 5, 2010
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status:  Prescription
Patent and Exclusivity Information

OXYCONTIN (OXYCODONE HYDROCHLORIDE)
15MG Marketing Status: Prescription

Active Ingredient: OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 15MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N022272
Product Number: 002
Approval Date: Apr 5, 2010
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status:  Prescription
Patent and Exclusivity Information

OXYCONTIN (OXYCODONE HYDROCHLORIDE)
20MG Marketing Status: Prescription

Active Ingredient: OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 20MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N022272
Product Number: 003
Approval Date: Apr 5, 2010
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status:  Prescription
Patent and Exclusivity Information

OXYCONTIN (OXYCODONE HYDROCHLORIDE)
30MG Marketing Status: Prescription

Active Ingredient: OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 30MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N022272
Product Number: 004
Approval Date: Apr 5, 2010
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status:  Prescription
Patent and Exclusivity Information

OXYCONTIN (OXYCODONE HYDROCHLORIDE)
40MG Marketing Status: Prescription

Active Ingredient: OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 40MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N022272
Product Number: 005
Approval Date: Apr 5, 2010
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status:  Prescription
Patent and Exclusivity Information

OXYCONTIN (OXYCODONE HYDROCHLORIDE)
60MG Marketing Status: Prescription

Active Ingredient: OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 60MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N022272
Product Number: 006
Approval Date: Apr 5, 2010
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status:  Prescription
Patent and Exclusivity Information

OXYCONTIN (OXYCODONE HYDROCHLORIDE)
80MG Marketing Status: Prescription

Active Ingredient: OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 80MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N022272
Product Number: 007
Approval Date: Apr 5, 2010
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status:  Prescription
Patent and Exclusivity Information

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