NDC 0054-0188 – Buprenorphine and naloxone
Buprenorphine Hydrochloride 2 mg/1; Naloxone Hydrochloride Dihydrate .5 mg/1 · Tablet · Sublingual
Product NDC0054-0188
Product details
- Brand name
- Buprenorphine and naloxone
- Generic name
- Buprenorphine and naloxone
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA203326
- Marketed since
- June 27, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 2 mg/1
- Naloxone Hydrochloride Dihydrate .5 mg/1
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0054-0188-13 | 30 TABLET in 1 BOTTLE (0054-0188-13) | Jun 27, 2014 |
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