NDC 63629-9475 – Buprenorphine

Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual

Human Prescription Drug DEA schedule CIII

Product NDC63629-9475

Product details

Brand name
Buprenorphine
Generic name
Buprenorphine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Sublingual
Marketing category
ANDA · ANDA207276
Marketed since
October 25, 2017
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
63629-9475-130 TABLET in 1 BOTTLE (63629-9475-1)Nov 28, 2022

Other Buprenorphine products