NDC 0406-1170 – Naltrexone Hydrochloride

Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0406-1170

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone hydrochloride
Labeler
SpecGx LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076264
Marketed since
March 22, 2002
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0406-1170-01100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01)Mar 22, 2002
0406-1170-0330 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03)Mar 22, 2002

Recalls mentioning this NDC

Other Naltrexone Hydrochloride products