Chlordiazepoxide Hydrochloride
- Product NDC
- 66267-771
- 11-digit product format
- 662670771
- Labeler code
- 66267
- Product ID
- 66267-771_9cbdbe41-12c8-6938-e053-2a95a90ae941
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA084769
- Marketing category
- ANDA
- Marketing start
- 1976-07-01
- Marketing end
- 0000-00-00
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66267-771-06 | 66267077106 | 6 CAPSULE in 1 BOTTLE (66267-771-06) | 6 capsule | 2017-02-15 | 0000-00-00 | No | No | Current |