NDC 72888-510 – Buprenorphine hydrochloride
Buprenorphine Hydrochloride 12 mg/1 · Tablet · Sublingual
Product NDC72888-510
Product details
- Brand name
- Buprenorphine hydrochloride
- Generic name
- Buprenorphine hydrochloride
- Labeler
- Advagen Pharma Ltd
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA090279
- Marketed since
- February 1, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 12 mg/1
Uses, dosage, side effects and warnings for Buprenorphine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72888-510-01 | 30 TABLET in 1 BOTTLE (72888-510-01) | Jul 10, 2026 |
| 72888-510-02 | 90 TABLET in 1 BOTTLE (72888-510-02) | Jul 10, 2026 |
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