Lorazepam
- Product NDC
- 51079-417
- 11-digit product format
- 510790417
- Labeler code
- 51079
- Product ID
- 51079-417_7e0417d6-3455-7def-e053-2a91aa0a7d22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA077657
- Marketing category
- ANDA
- Marketing start
- 2006-12-27
- Marketing end
- 0000-00-00
- Substance
- LORAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record