Clonazepam
- Product NDC
- 71205-252
- 11-digit product format
- 712050252
- Labeler code
- 71205
- Product ID
- 71205-252_a0bca6db-e332-4b67-b763-82ba14855bc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA074869
- Marketing category
- ANDA
- Marketing start
- 1997-02-12
- Marketing end
- 0000-00-00
- Substance
- CLONAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-252 | CLONAZEPAM TABLET [PROFICIENT RX LP] | 2 | Legacy NDC | 20191010_d66f9488-e881-4940-af8b-eca13ab3f197.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-252-30 | 71205025230 | 30 TABLET in 1 BOTTLE (71205-252-30) | 30 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 71205-252-60 | 71205025260 | 60 TABLET in 1 BOTTLE (71205-252-60) | 60 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |
| 71205-252-90 | 71205025290 | 90 TABLET in 1 BOTTLE (71205-252-90) | 90 tablet | 2019-04-01 | 0000-00-00 | No | No | Current |