NDC 60687-637 – Buprenorphine and Naloxone
Buprenorphine Hydrochloride 8 mg/1; Naloxone Hydrochloride Dihydrate 2 mg/1 · Tablet · Sublingual
Product NDC60687-637
Product details
- Brand name
- Buprenorphine and Naloxone
- Generic name
- Buprenorphine and Naloxone
- Labeler
- American Health Packaging
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA205601
- Marketed since
- March 14, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 60687-637-65 | 50 BLISTER PACK in 1 CARTON (60687-637-65) / 1 TABLET in 1 BLISTER PACK (60687-637-11) | Mar 14, 2022 |
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