NDC 62756-970 – Buprenorphine and Naloxone
Buprenorphine Hydrochloride 8 mg/1; Naloxone Hydrochloride Dihydrate 2 mg/1 · Tablet · Sublingual
Product NDC62756-970
Product details
- Brand name
- Buprenorphine and Naloxone
- Generic name
- Buprenorphine and Naloxone
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA201633
- Marketed since
- July 18, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62756-970-64 | 3 BLISTER PACK in 1 CARTON (62756-970-64) / 10 TABLET in 1 BLISTER PACK | Jul 18, 2017 |
| 62756-970-83 | 30 TABLET in 1 BOTTLE (62756-970-83) | Jul 18, 2017 |
Recalls mentioning this NDC
- D-0024-2023 Nov 9, 2022 · Class II
Presence of Foreign Substance
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