Buprenorphine HCl
- Product NDC
- 67046-998
- 11-digit product format
- 670460998
- Labeler code
- 67046
- Product ID
- 67046-998_593c9ffe-e96e-d873-e053-2a91aa0a0e19
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buprenorphine HCl
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA078633
- Marketing category
- ANDA
- Marketing start
- 2009-10-08
- Marketing end
- 0000-00-00
- Substance
- BUPRENORPHINE HYDROCHLORIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record