Chlordiazepoxide Hydrochloride
- Product NDC
- 60429-555
- 11-digit product format
- 604290555
- Labeler code
- 60429
- Product ID
- 60429-555_c59dc331-96dc-6469-e053-2995a90a8f51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA085472
- Marketing category
- ANDA
- Marketing start
- 1982-01-01
- Marketing end
- 0000-00-00
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 60429-555-01 | 60429055501 | 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (60429-555-01) | 2011-08-12 | 0000-00-00 | No | No | Current |