Chlordiazepoxide Hydrochloride
- Product NDC
- 63629-4669
- 11-digit product format
- 636294669
- Labeler code
- 63629
- Product ID
- 63629-4669_041c8d6d-7f4a-4a89-a086-622002e425d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA083116
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4669-1 | 63629466901 | 30 CAPSULE in 1 BOTTLE (63629-4669-1) | 30 capsule | 2012-02-10 | 0000-00-00 | No | No | Current |
| 63629-4669-2 | 63629466902 | 90 CAPSULE in 1 BOTTLE (63629-4669-2) | 90 capsule | 2013-09-27 | 0000-00-00 | No | No | Current |
| 63629-4669-3 | 63629466903 | 60 CAPSULE in 1 BOTTLE (63629-4669-3) | 60 capsule | 2013-10-25 | 0000-00-00 | No | No | Current |