NDC 58118-1189-8
buprenorphine hydrochloride and naloxone hydrochloride dihydrate 8 mg/1
buprenorphine hydrochloride and naloxone hydrochloride dihydrate · TABLET
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 Clinical Solutions Wholesale, LLC.
Key Facts
- Brand Name
- buprenorphine hydrochloride and naloxone hydrochloride dihydrate
- Generic Name
- buprenorphine hydrochloride and naloxone hydrochloride dihydrate
- NDC Code (Package)
58118-1189-8- NDC Code (Product)
58118-1189- Manufacturer
- Clinical Solutions Wholesale, LLC
- Strength
- 8 mg/1
- Dosage Form
- TABLET
- Route
- SUBLINGUAL
- Marketing Status
- DEA Schedule
- Schedule III (Controlled)
- Application #
- ANDA203326
- Marketing Start
- 06/27/2014
Recall History
No Recall HistoryNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.