Chlordiazepoxide Hydrochloride
- Product NDC
- 70518-3134
- 11-digit product format
- 705183134
- Labeler code
- 70518
- Product ID
- 70518-3134_c59751f2-8e9e-647c-e053-2995a90ad25d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084768
- Marketing category
- ANDA
- Marketing start
- 2021-06-24
- Marketing end
- 0000-00-00
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| MFM6K1XWDK | CHLORDIAZEPOXIDE HYDROCHLORIDE | 438-41-5 | CHLORDIAZEPOXIDE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3134-0 | 70518313400 | 30 CAPSULE in 1 BLISTER PACK (70518-3134-0) | 30 capsule | 2021-06-24 | 0000-00-00 | No | No | Current |