Chlordiazepoxide Hydrochloride
- Product NDC
- 63629-3725
- 11-digit product format
- 636293725
- Labeler code
- 63629
- Product ID
- 63629-3725_2a82fbd9-5867-4188-97b9-509f33299f80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA084768
- Marketing category
- ANDA
- Marketing start
- 1976-07-01
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 63629-3725-1 | 63629372501 | 30 CAPSULE in 1 BOTTLE (63629-3725-1) | 30 capsule | 2024-05-29 | No | No | Historical |
| 63629-3725-2 | 63629372502 | 60 CAPSULE in 1 BOTTLE (63629-3725-2) | 60 capsule | 2024-05-29 | No | No | Historical |