NDC 0054-0177 – Buprenorphine

Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC0054-0177

Product details

Brand name
Buprenorphine
Generic name
Buprenorphine
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA078633
Marketed since
October 8, 2009
Listing expires
December 31, 2027
Pharmacologic class
Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Buprenorphine →

Package NDC codes (1)

Package NDCDescriptionSince
0054-0177-1330 TABLET in 1 BOTTLE (0054-0177-13)Oct 8, 2009

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