Clorazepate Dipotassium
- Product NDC
- 43063-030
- 11-digit product format
- 430630030
- Labeler code
- 43063
- Product ID
- 43063-030_dafe0df3-20fe-0a35-e053-2a95a90a9011
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clorazepate dipotassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA071858
- Marketing category
- ANDA
- Marketing start
- 1987-07-17
- Marketing end
- 0000-00-00
- Substance
- CLORAZEPATE DIPOTASSIUM
- Active strength
- 15 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 43063-030-03 | 43063003003 | 3 TABLET in 1 BOTTLE, PLASTIC (43063-030-03) | 3 tablet | 2010-06-17 | 0000-00-00 | No | No | Current |
| 43063-030-06 | 43063003006 | 6 TABLET in 1 BOTTLE, PLASTIC (43063-030-06) | 6 tablet | 2010-06-17 | 0000-00-00 | No | No | Current |
| 43063-030-10 | 43063003010 | 10 TABLET in 1 BOTTLE, PLASTIC (43063-030-10) | 10 tablet | 2010-06-17 | 0000-00-00 | No | No | Current |
| 43063-030-12 | 43063003012 | 12 TABLET in 1 BOTTLE, PLASTIC (43063-030-12) | 12 tablet | 2010-06-17 | 0000-00-00 | No | No | Current |