Buprenorphine And Naloxone 43598-0581
Product NDC
43598-0581- Manufacturer
- Dr.reddys Laboratories Inc
- Dosage Form
- Film, Soluble
- Route
- Buccal And Sublingual
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- June 14, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA205806
Active Ingredients
| Ingredient | Strength |
|---|---|
| Buprenorphine Hydrochloride | 12 mg/1 |
| Naloxone | 3 mg/1 |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(1)
30 POUCH in 1 CARTON (43598-581-30) / 1 FILM, SOLUBLE in 1 POUCH (43598-581-01)