NDC 62756-460 – Buprenorphine
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC62756-460
Product details
- Brand name
- Buprenorphine
- Generic name
- Buprenorphine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA201760
- Marketed since
- February 17, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 8 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62756-460-64 | 3 BLISTER PACK in 1 CARTON (62756-460-64) / 10 TABLET in 1 BLISTER PACK | Feb 17, 2016 |
| 62756-460-83 | 30 TABLET in 1 BOTTLE (62756-460-83) | Feb 17, 2016 |
Recalls mentioning this NDC
- D-0869-2023 Jun 14, 2023 · Class II
CGMP Deviations
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