Chlordiazepoxide Hydrochloride
- Product NDC
- 50090-0328
- 11-digit product format
- 500900328
- Labeler code
- 50090
- Product ID
- 50090-0328_86950e87-375c-401e-b690-94ad639dc496
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2022-12-31
- 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 |
|---|
| 50090-0328-3 | 50090032803 | 30 CAPSULE in 1 BOTTLE (50090-0328-3) | 30 capsule | 2014-03-26 | 0000-00-00 | No | No | Current |