NDC 71335-3152 – Buprenorphine
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC71335-3152
Product details
- Brand name
- Buprenorphine
- Generic name
- Buprenorphine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA201760
- Marketed since
- February 17, 2016
- 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 |
|---|---|---|
| 71335-3152-0 | 120 TABLET in 1 BOTTLE (71335-3152-0) | Jun 29, 2026 |
| 71335-3152-1 | 90 TABLET in 1 BOTTLE (71335-3152-1) | Jun 29, 2026 |
| 71335-3152-2 | 60 TABLET in 1 BOTTLE (71335-3152-2) | Jun 29, 2026 |
| 71335-3152-3 | 30 TABLET in 1 BOTTLE (71335-3152-3) | Jun 29, 2026 |
| 71335-3152-4 | 20 TABLET in 1 BOTTLE (71335-3152-4) | Jun 29, 2026 |
| 71335-3152-5 | 7 TABLET in 1 BOTTLE (71335-3152-5) | Jun 29, 2026 |
| 71335-3152-6 | 28 TABLET in 1 BOTTLE (71335-3152-6) | Jun 29, 2026 |
| 71335-3152-7 | 1 TABLET in 1 BOTTLE (71335-3152-7) | Jun 29, 2026 |
| 71335-3152-8 | 12 TABLET in 1 BOTTLE (71335-3152-8) | Jun 29, 2026 |
| 71335-3152-9 | 14 TABLET in 1 BOTTLE (71335-3152-9) | Jun 29, 2026 |
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