NDC 71335-1154 – Buprenorphine
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC71335-1154
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, 2027
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 8 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1154-0 | 120 TABLET in 1 BOTTLE (71335-1154-0) | Apr 3, 2024 |
| 71335-1154-1 | 90 TABLET in 1 BOTTLE (71335-1154-1) | Mar 15, 2019 |
| 71335-1154-2 | 60 TABLET in 1 BOTTLE (71335-1154-2) | Mar 15, 2019 |
| 71335-1154-3 | 30 TABLET in 1 BOTTLE (71335-1154-3) | Jul 22, 2019 |
| 71335-1154-4 | 20 TABLET in 1 BOTTLE (71335-1154-4) | Apr 3, 2024 |
| 71335-1154-5 | 7 TABLET in 1 BOTTLE (71335-1154-5) | Jan 16, 2020 |
| 71335-1154-6 | 28 TABLET in 1 BOTTLE (71335-1154-6) | Jun 28, 2021 |
| 71335-1154-7 | 1 TABLET in 1 BOTTLE (71335-1154-7) | Apr 3, 2024 |
| 71335-1154-8 | 12 TABLET in 1 BOTTLE (71335-1154-8) | Apr 3, 2024 |
| 71335-1154-9 | 14 TABLET in 1 BOTTLE (71335-1154-9) | Apr 3, 2024 |
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