Klonopin
- Product NDC
- 61269-620
- 11-digit product format
- 612690620
- Labeler code
- 61269
- Product ID
- 61269-620_63cfdab9-fb3d-4c2b-bf88-8ba841dba839
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H2-Pharma, LLC
- Application
- NDA017533
- Marketing category
- NDA
- Marketing start
- 1975-06-02
- Substance
- CLONAZEPAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Klonopin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLONAZEPAM | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5PE9FDE8GB |
| Rxcui | 197527, 197528, 197529, 206157, 206159, 206160 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61269-620-10 | Klonopin | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61269-620 | KLONOPIN (CLONAZEPAM) TABLET [H2-PHARMA, LLC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241205_cfa0d79a-843c-4b88-95a1-e9511d649ca1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61269-620-10 | 61269062010 | 100 TABLET in 1 BOTTLE, PLASTIC (61269-620-10) | 100 tablet | 2010-08-26 | 0000-00-00 | No | No | Current |