Lorazepam
- Product NDC
- 53002-7720
- 11-digit product format
- 530027720
- Labeler code
- 53002
- Product ID
- 53002-7720_a817dada-c4bc-44c4-8a35-878e04c82b52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, 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
- 2021-12-31
- 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 |
|---|
| 53002-7720-1 | 53002772001 | 10 TABLET in 1 BOTTLE (53002-7720-1) | 10 tablet | 2017-10-01 | 0000-00-00 | No | No | Current |
| 53002-7720-2 | 53002772002 | 20 TABLET in 1 BOTTLE (53002-7720-2) | 20 tablet | 2017-10-01 | 0000-00-00 | No | No | Current |
| 53002-7720-3 | 53002772003 | 30 TABLET in 1 BOTTLE (53002-7720-3) | 30 tablet | 2017-10-01 | 0000-00-00 | No | No | Current |