Clonazepam
- Product NDC
- 50090-2823
- 11-digit product format
- 500902823
- Labeler code
- 50090
- Product ID
- 50090-2823_4d165335-1d0b-47c4-bcb1-ad761fda25ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2019-12-31
- 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 |
|---|
| 50090-2823-0 | Clonazepam | 33 in 1 BOTTLE | TABLET | 33 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2823 | CLONAZEPAM TABLET [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC, 1 package rows | 20181214_68bf5bfa-8357-44ed-82ff-ad80a11789c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2823-0 | 50090282300 | 33 in 1 BOTTLE | Historical |