NDC 0406-5755 – Methadone Hydrochloride

Methadone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC0406-5755

Product details

Brand name
Methadone Hydrochloride
Generic name
Methadone Hydrochloride
Labeler
SpecGx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040517
Marketed since
April 27, 2004
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0406-5755-01100 TABLET in 1 BOTTLE (0406-5755-01)Apr 27, 2004
0406-5755-231 TABLET in 1 BLISTER PACK (0406-5755-23)Apr 27, 2004
0406-5755-62100 TABLET in 1 BLISTER PACK (0406-5755-62)Apr 27, 2004

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