Chlordiazepoxide Hydrochloride
- Product NDC
- 43547-251
- 11-digit product format
- 435470251
- Labeler code
- 43547
- Product ID
- 43547-251_9653dfb9-2fe1-48e3-8b77-44f6eef703fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Solco Healthcare US LLC
- Application
- ANDA085461
- Marketing category
- ANDA
- Marketing start
- 2010-05-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43547-251-10 | 43547025110 | 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (43547-251-10) | 2010-05-15 | 0000-00-00 | No | No | Current |