Lorazepam
- Product NDC
- 68071-5061
- 11-digit product format
- 680715061
- Labeler code
- 68071
- Product ID
- 68071-5061_bbb67b5b-d96a-9eca-e053-2a95a90ab5af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA072927
- Marketing category
- ANDA
- Marketing start
- 1991-10-31
- 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
- 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 |
|---|
| 68071-5061-6 | 68071506106 | 6 TABLET in 1 BOTTLE (68071-5061-6) | 6 tablet | 2019-09-16 | 0000-00-00 | No | No | Current |