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OxycontinDrug - Oxycontin The trade name of the product as shown on the labeling.
Dosage -
TABLET, EXTENDED RELEASE; ORAL
Active Ingredient(s) -
Oxycodone Hydrochloride
Strength -
20MG
Applicant -
PURDUE PHARMA LP
New Drug Application (NDA) Number -
020553
Product Number -
002
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Dec 12, 1995
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Purdue Pharma Lp
Oxycontin
Oxybutynin Chloride 5mg Tablet; Oral
Oxycodone Hcl 10mg Tablet, Extended Release; Oral Oxycodone Hcl 20mg Tablet, Extended Release; Oral Oxycodone Hcl 40mg Tablet, Extended Release; Oral Oxycodone Hcl 80mg Tablet, Extended Release; Oral Oxycodone Hcl 80mg Tablet, Extended Release; Oral Oxycodone Hcl 80mg Tablet, Extended Release; Oral Oxycontin 10mg Tablet, Extended Release; Oral Oxycontin 160mg Tablet, Extended Release; Oral Oxycontin 20mg Tablet, Extended Release; Oral NewDrugInformation |