Clonazepam
- Product NDC
- 50436-2948
- 11-digit product format
- 504362948
- Labeler code
- 50436
- Product ID
- 50436-2948_73f867a1-3da9-4c6f-8f57-d337d237af2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077856
- Marketing category
- ANDA
- Marketing start
- 2006-06-28
- 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-2948-1 | Clonazepam | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 50436-2948-2 | Clonazepam | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-2948 | CLONAZEPAM TABLET [UNIT DOSE SERVICES] | 3 | Legacy NDC, 2 package rows | 20170702_50a46bd0-d57e-4685-a027-622f63bfcf80.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-2948-1 | 50436294801 | 30 in 1 BOTTLE | Historical |
| 50436-2948-2 | 50436294802 | 60 in 1 BOTTLE | Historical |