NDCFind

Buprenorphine And Naloxone 50742-0398-30

Package NDC

50742-0398-30

Product NDC: 50742-0398

Manufacturer
Ingenus Pharmaceuticals, Llc
Dosage Form
Film
Route
Buccal And Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
August 29, 2023
Listing Expires
December 31, 2027
Application
ANDA212756

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride4 mg/1
Naloxone Hydrochloride1 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]Partial Opioid Agonist [EPC]

Selected Package

50742-0398-30Selected

30 POUCH in 1 CARTON (50742-398-30) / 1 FILM in 1 POUCH (50742-398-01)