Clonazepam
- Product NDC
- 60687-555
- 11-digit product format
- 606870555
- Labeler code
- 60687
- Product ID
- 60687-555_e41af6bd-28f1-d7f1-e053-2995a90a831e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA074569
- Marketing category
- ANDA
- Marketing start
- 2020-08-20
- 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
- 2023-12-31
- 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 |
|---|
| 60687-555 | CLONAZEPAM TABLET [AMERICAN HEALTH PACKAGING] | 5 | Legacy NDC | 20240828_cd7b7c4d-8dd1-4a0a-a506-a84407816bdf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-555-01 | 60687055501 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-555-01) > 1 TABLET in 1 BLISTER PACK (60687-555-11) | 100 blister pack | 2020-06-01 | 0000-00-00 | No | No | Current |