NDCFind

Oxycodone Hydrochloride 70752-0137-03

Package NDC

70752-0137-03

Product NDC: 70752-0137

Manufacturer
Quagen Pharmaceuticals Llc
Dosage Form
Solution
Route
Oral
Product Type
Human Prescription Drug
DEA Schedule
Schedule CII
Marketing Start
June 2, 2021
Listing Expires
December 31, 2026
Application
ANDA213761

Active Ingredients

IngredientStrength
Oxycodone Hydrochloride100 mg/5mL

Drug Class

Full Opioid Agonists [MoA]Opioid Agonist [EPC]

Selected Package

70752-0137-03Selected

1 BOTTLE in 1 CARTON (70752-137-03) / 30 mL in 1 BOTTLE