NDC 0054-0709 – Methadone Hydrochloride

Methadone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC0054-0709

Product details

Brand name
Methadone Hydrochloride
Generic name
Methadone Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA088109
Marketed since
March 8, 1983
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0054-0709-201 BLISTER PACK in 1 CARTON (0054-0709-20) / 100 TABLET in 1 BLISTER PACKMar 8, 1983
0054-0709-25100 TABLET in 1 BOTTLE, PLASTIC (0054-0709-25)Mar 8, 1983

Recalls mentioning this NDC

Other Methadone Hydrochloride products