buprenorphine hydrochloride
- Product NDC
- 50090-1571
- 11-digit product format
- 500901571
- Labeler code
- 50090
- Product ID
- 50090-1571_41aabd23-353d-4934-8584-74a01d31017f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- buprenorphine hydrochloride
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090622
- Marketing category
- ANDA
- Marketing start
- 2010-09-24
- Marketing end
- 0000-00-00
- Substance
- BUPRENORPHINE HYDROCHLORIDE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1571-0 | 50090157100 | 30 TABLET in 1 BOTTLE (50090-1571-0) | 30 tablet | 2014-12-23 | 0000-00-00 | No | No | Current |