Lorazepam
- Product NDC
- 70518-1313
- 11-digit product format
- 705181313
- Labeler code
- 70518
- Product ID
- 70518-1313_922ec0fb-1c0f-63b6-e053-2995a90a9677
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072926
- Marketing category
- ANDA
- Marketing start
- 2018-07-19
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record