Lorazepam
- Product NDC
- 70934-782
- 11-digit product format
- 709340782
- Labeler code
- 70934
- Product ID
- 70934-782_ac9caebd-e190-a27c-e053-2995a90aec96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA203572
- Marketing category
- ANDA
- Marketing start
- 2020-07-15
- 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 |
|---|
| 70934-782-10 | 70934078210 | 10 TABLET in 1 BOTTLE, PLASTIC (70934-782-10) | 10 tablet | 2020-07-15 | 0000-00-00 | No | No | Current |