NDC 0406-0512 – Oxycodone And Acetaminophen

Oxycodone Hydrochloride 5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 2 recalls

Product NDC0406-0512

Product details

Brand name
Oxycodone And Acetaminophen
Generic name
oxycodone hydrochloride and acetaminophen
Labeler
SpecGx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA087463
Marketed since
December 7, 1983
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Oxycodone And Acetaminophen →

Package NDC codes (5)

Package NDCDescriptionSince
0406-0512-01100 TABLET in 1 BOTTLE (0406-0512-01)Dec 7, 1983
0406-0512-05500 TABLET in 1 BOTTLE (0406-0512-05)Dec 7, 1983
0406-0512-231 TABLET in 1 BLISTER PACK (0406-0512-23)Dec 7, 1983
0406-0512-62100 TABLET in 1 BLISTER PACK (0406-0512-62)Dec 7, 1983
0406-0512-915000 TABLET in 1 PAIL (0406-0512-91)Dec 7, 1983

Recalls mentioning this NDC

Other Oxycodone And Acetaminophen products