NDC 0054-0176 – Buprenorphine
Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual
Product NDC0054-0176
Product details
- Brand name
- Buprenorphine
- Generic name
- Buprenorphine
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA078633
- Marketed since
- October 8, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 2 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0054-0176-13 | 30 TABLET in 1 BOTTLE (0054-0176-13) | Oct 8, 2009 |
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