Drugplain

NDC 70518-3844-0

buprenorphine hydrochloride and naloxone hydrochloride dihydrate 8 mg/1

buprenorphine hydrochloride and naloxone hydrochloride dihydrate · TABLET

No Recall History

buprenorphine hydrochloride and naloxone hydrochloride dihydrate is a tablet containing buprenorphine hydrochloride and naloxone hydrochloride dihydrate at a strength of 8 mg/1. Manufactured by REMEDYREPACK INC..

Key Facts

Brand Name
buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Generic Name
buprenorphine hydrochloride and naloxone hydrochloride dihydrate
NDC Code (Package)
70518-3844-0
NDC Code (Product)
70518-3844
Manufacturer
REMEDYREPACK INC.
Strength
8 mg/1
Dosage Form
TABLET
Route
SUBLINGUAL
Marketing Status
DEA Schedule
Schedule III (Controlled)
Application #
ANDA203326
Marketing Start
08/29/2023

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.