Clorazepate Dipotassium
- Product NDC
- 0378-0030
- 11-digit product format
- 003780030
- Labeler code
- 0378
- Product ID
- 0378-0030_21627ba9-f1e6-4251-b3fc-8836c1f7266f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clorazepate dipotassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA071858
- Marketing category
- ANDA
- Marketing start
- 1987-07-17
- Marketing end
- 0000-00-00
- Substance
- CLORAZEPATE DIPOTASSIUM
- Active strength
- 4 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-0030-01 | 00378003001 | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0030-01) | 100 tablet | 1987-07-17 | 0000-00-00 | No | No | Current |
| 0378-0030-05 | 00378003005 | 500 TABLET in 1 BOTTLE, PLASTIC (0378-0030-05) | 500 tablet | 1987-07-17 | 0000-00-00 | No | No | Current |