Clobazam
- Product NDC
- 72606-004
- 11-digit product format
- 726060004
- Labeler code
- 72606
- Product ID
- 72606-004_19cd2331-75e7-4fb1-a439-d4524a9bd68f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clobazam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CELLTRION USA, INC.
- Application
- ANDA211959
- Marketing category
- ANDA
- Marketing start
- 2021-01-21
- 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
- 2022-12-31
- 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 |
|---|
| 72606-004-01 | 72606000401 | 1 BOTTLE in 1 CARTON (72606-004-01) > 100 TABLET in 1 BOTTLE | 1 bottle | 2021-01-21 | 0000-00-00 | No | No | Current |