NDC 71335-0950 – Buprenorphine
Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual
Product NDC71335-0950
Product details
- Brand name
- Buprenorphine
- Generic name
- Buprenorphine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA207276
- Marketed since
- October 25, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 2 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0950-1 | 60 TABLET in 1 BOTTLE (71335-0950-1) | Sep 13, 2018 |
| 71335-0950-2 | 90 TABLET in 1 BOTTLE (71335-0950-2) | Sep 13, 2018 |
| 71335-0950-3 | 30 TABLET in 1 BOTTLE (71335-0950-3) | Sep 23, 2022 |
| 71335-0950-4 | 7 TABLET in 1 BOTTLE (71335-0950-4) | Sep 23, 2022 |
| 71335-0950-5 | 28 TABLET in 1 BOTTLE (71335-0950-5) | Sep 23, 2022 |
| 71335-0950-6 | 1 TABLET in 1 BOTTLE (71335-0950-6) | Sep 23, 2022 |
| 71335-0950-7 | 12 TABLET in 1 BOTTLE (71335-0950-7) | Sep 23, 2022 |
| 71335-0950-8 | 120 TABLET in 1 BOTTLE (71335-0950-8) | Sep 23, 2022 |
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