Clonazepam
- Product NDC
- 70518-2485
- 11-digit product format
- 705182485
- Labeler code
- 70518
- Product ID
- 70518-2485_f1741314-b826-db5b-e053-2995a90aac04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077856
- Marketing category
- ANDA
- Marketing start
- 2019-12-13
- Marketing end
- 0000-00-00
- Substance
- CLONAZEPAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2485-0 | 70518248500 | 30 TABLET in 1 BLISTER PACK (70518-2485-0) | 30 tablet | 2019-12-13 | 0000-00-00 | No | No | Current |
| 70518-2485-1 | 70518248501 | 100 POUCH in 1 BOX (70518-2485-1) > 1 TABLET in 1 POUCH (70518-2485-2) | 100 pouch | 2020-07-15 | 0000-00-00 | No | No | Current |
| 70518-2485-3 | 70518248503 | 100 POUCH in 1 BOX (70518-2485-3) > 1 TABLET in 1 POUCH (70518-2485-4) | 100 pouch | 2021-02-10 | 0000-00-00 | No | No | Current |