NDC 43598-581 – Buprenorphine and Naloxone
Buprenorphine Hydrochloride 12 mg/1; Naloxone 3 mg/1 · Film, Soluble · Buccal, Sublingual
Product NDC43598-581
Product details
- Brand name
- Buprenorphine and Naloxone
- Generic name
- Buprenorphine and Naloxone
- Labeler
- Dr.Reddys Laboratories Inc
- Dosage form
- Film, Soluble
- Route
- Buccal, Sublingual
- Marketing category
- ANDA · ANDA205806
- Marketed since
- June 14, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 12 mg/1
- Naloxone 3 mg/1
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 43598-581-30 | 30 POUCH in 1 CARTON (43598-581-30) / 1 FILM, SOLUBLE in 1 POUCH (43598-581-01) | Jun 14, 2018 |
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