NDC 0054-0189-13
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 Hikma Pharmaceuticals USA Inc..
Key Facts
- Brand Name
- buprenorphine hydrochloride and naloxone hydrochloride dihydrate
- Generic Name
- buprenorphine hydrochloride and naloxone hydrochloride dihydrate
- NDC Code (Package)
0054-0189-13- NDC Code (Product)
0054-0189- Manufacturer
- Hikma Pharmaceuticals USA Inc.
- 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.