OxyContin - oxycodone hydrochloride
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Field |
Value |
NDC Code: |
10544-591 |
Proprietary Name: |
OxyContin |
Suffix: |
|
Non-Proprietary Name: |
oxycodone hydrochloride |
Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
Method: |
ORAL |
Original Marketing Date: |
26-01-2010 |
Category Name: |
NDA |
Application Number: |
NDA020553 |
Labeler: |
BLENHEIM PHARMACAL, INC. |
Substance Name: |
OXYCODONE HYDROCHLORIDE |
Active Numerator Strength: |
10 |
Active Ingredient Unit: |
mg/1 |
Pharm Classes: |
Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule: |
CII |