NDC 10702-018 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC10702-018

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
KVK-TECH,INC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091393
Marketed since
October 18, 2013
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
10702-018-01100 TABLET in 1 BOTTLE (10702-018-01)Oct 18, 2013
10702-018-50500 TABLET in 1 BOTTLE (10702-018-50)Oct 18, 2013

Recalls mentioning this NDC

Other Oxycodone Hydrochloride products