NDCFind

Oxycodone Hydrochloride 71930-0022-43

Package NDC

71930-0022-43

Product NDC: 71930-0022

Manufacturer
Eywa Pharma Inc
Dosage Form
Solution
Route
Oral
Product Type
Human Prescription Drug
DEA Schedule
Schedule CII
Marketing Start
March 1, 2019
Listing Expires
December 31, 2027
Application
ANDA207511

Active Ingredients

IngredientStrength
Oxycodone Hydrochloride5 mg/5mL

Drug Class

Full Opioid Agonists [MoA]Opioid Agonist [EPC]

Selected Package

71930-0022-43Selected

1 BOTTLE in 1 CARTON (71930-022-43) / 473 mL in 1 BOTTLE