Clobazam
- Product NDC
- 69452-115
- 11-digit product format
- 694520115
- Labeler code
- 69452
- Product ID
- 69452-115_f1ed5637-3115-3407-e053-2a95a90a83a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobazam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bionpharma Inc.
- Application
- ANDA208825
- Marketing category
- ANDA
- Marketing start
- 2017-10-20
- Marketing end
- 0000-00-00
- Substance
- CLOBAZAM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 69452-115-20 | 69452011520 | 100 TABLET in 1 BOTTLE (69452-115-20) | 100 tablet | 2018-10-22 | 0000-00-00 | No | No | Current |