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Oxycodone Hydrochloride - Oxycodone Hydrochloride

Navigation: NDC > Supplier starting with: Q > QUALITEST PHARMACEUTICALS
Field Value
NDC Code: 0603-4991
Proprietary Name: Oxycodone Hydrochloride
Suffix:
Non-Proprietary Name: Oxycodone Hydrochloride
Dosage Form: TABLET
Method: ORAL
Original Marketing Date: 31-01-2007
Category Name: ANDA
Application Number: ANDA077712
Labeler: QUALITEST PHARMACEUTICALS
Substance Name: OXYCODONE HYDROCHLORIDE
Active Numerator Strength: 15
Active Ingredient Unit: mg/1
Pharm Classes: Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA Schedule: CII