NDC 43598-581-30
Buprenorphine and Naloxone 12 mg/1
Buprenorphine and Naloxone · FILM, SOLUBLE
Buprenorphine and Naloxone is a film, soluble containing buprenorphine and naloxone at a strength of 12 mg/1. Manufactured by Dr.Reddys Laboratories Inc.
Key Facts
- Brand Name
- Buprenorphine and Naloxone
- Generic Name
- Buprenorphine and Naloxone
- NDC Code (Package)
43598-581-30- NDC Code (Product)
43598-581- Manufacturer
- Dr.Reddys Laboratories Inc
- Strength
- 12 mg/1
- Dosage Form
- FILM, SOLUBLE
- Route
- BUCCAL, SUBLINGUAL
- Marketing Status
- DEA Schedule
- Schedule III (Controlled)
- Application #
- ANDA205806
- Drug Class
- Opioid Antagonist [EPC]
- Marketing Start
- 06/14/2018
Recall History
No Recall HistoryView Full Drug Page
Buprenorphine and Naloxone — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.