Lorazepam
- Product NDC
- 43063-057
- 11-digit product format
- 430630057
- Labeler code
- 43063
- Product ID
- 43063-057_d5f2ebdc-ec4c-57bf-e053-2a95a90a58e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072926
- Marketing category
- ANDA
- Marketing start
- 1991-10-31
- Marketing end
- 2023-04-30
- Substance
- LORAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-057-06 | 43063005706 | 6 TABLET in 1 BOTTLE, PLASTIC (43063-057-06) | 6 tablet | 2010-08-04 | 0000-00-00 | No | No | Current |