NDC 0406-0552 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC0406-0552

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone hydrochloride
Labeler
SpecGx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076758
Marketed since
June 30, 2004
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0406-0552-01100 TABLET in 1 BOTTLE (0406-0552-01)Jun 30, 2004
0406-0552-231 TABLET in 1 BLISTER PACK (0406-0552-23)Jun 30, 2004
0406-0552-62100 TABLET in 1 BLISTER PACK (0406-0552-62)Jun 30, 2004

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