Clonazepam
- Product NDC
- 70518-1353
- 11-digit product format
- 705181353
- Labeler code
- 70518
- Product ID
- 70518-1353_e8b9af92-da02-6f06-e053-2a95a90ab92c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077856
- Marketing category
- ANDA
- Marketing start
- 2018-08-08
- 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 |
|---|
| 70518-1353 | CLONAZEPAM TABLET [REMEDYREPACK INC.] | 14 | Legacy NDC | 20250511_bca43c08-2141-4c02-95d4-01756557b6c2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1353-0 | 70518135300 | 30 TABLET in 1 BLISTER PACK (70518-1353-0) | 30 tablet | 2018-08-08 | 0000-00-00 | No | No | Current |
| 70518-1353-1 | 70518135301 | 100 POUCH in 1 BOX (70518-1353-1) > 1 TABLET in 1 POUCH (70518-1353-2) | 100 pouch | 2019-12-16 | 0000-00-00 | No | No | Current |