NDC 0904-7155 – Buprenorphine
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC0904-7155
Product details
- Brand name
- Buprenorphine
- Generic name
- Buprenorphine
- Labeler
- Major Pharmaceuticals
- 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 8 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0904-7155-04 | 30 BLISTER PACK in 1 CARTON (0904-7155-04) / 1 TABLET in 1 BLISTER PACK | Oct 8, 2009 |
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