NDC 67296-2191 – BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE
Buprenorphine Hydrochloride 8 mg/1; Naloxone Hydrochloride Dihydrate 2 mg/1 · Tablet · Sublingual
Product NDC67296-2191
Product details
- Brand name
- BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE
- Generic name
- BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE
- Labeler
- Redpharm Drug
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA209069
- Marketed since
- September 1, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 67296-2191-1 | 12 TABLET in 1 BOTTLE, PLASTIC (67296-2191-1) | Sep 1, 2020 |
| 67296-2191-6 | 6 TABLET in 1 BOTTLE, PLASTIC (67296-2191-6) | Sep 1, 2020 |
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