NDC 50742-397 – Buprenorphine and Naloxone
Buprenorphine Hydrochloride 2 mg/1; Naloxone Hydrochloride .5 mg/1 · Film · Buccal, Sublingual
Product NDC50742-397
Product details
- Brand name
- Buprenorphine and Naloxone
- Generic name
- Buprenorphine and naloxone
- Labeler
- INGENUS PHARMACEUTICALS, LLC
- Dosage form
- Film
- Route
- Buccal, Sublingual
- Marketing category
- ANDA · ANDA212756
- Marketed since
- August 29, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 2 mg/1
- Naloxone Hydrochloride .5 mg/1
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50742-397-30 | 30 POUCH in 1 CARTON (50742-397-30) / 1 FILM in 1 POUCH (50742-397-01) | Aug 8, 2024 |
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