NDC 42858-502 – Buprenorphine
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC42858-502
Product details
- Brand name
- Buprenorphine
- Generic name
- Buprenorphine
- Labeler
- Rhodes Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA207276
- Marketed since
- October 25, 2017
- 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 |
|---|---|---|
| 42858-502-03 | 30 TABLET in 1 BOTTLE (42858-502-03) | Oct 25, 2017 |
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