NDC 58118-8020 – Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
Buprenorphine Hydrochloride 8 mg/1; Naloxone Hydrochloride Dihydrate 2 mg/1 · Tablet · Sublingual
Product NDC58118-8020
Product details
- Brand name
- Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
- Generic name
- Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
- Labeler
- Clinical Solutions Wholesale, LLC
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA207000
- Marketed since
- December 13, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 58118-8020-8 | 30 TABLET in 1 BLISTER PACK (58118-8020-8) | Jul 11, 2023 |
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