Chlordiazepoxide Hydrochloride
- Product NDC
- 55154-5652
- 11-digit product format
- 551545652
- Labeler code
- 55154
- Product ID
- 55154-5652_11b0ba86-e1a1-4be8-a7ea-c343a123ff5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA084769
- Marketing category
- ANDA
- Marketing start
- 2011-04-01
- 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
- 2020-12-31
- 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 |
|---|
| 55154-5652-0 | 55154565200 | 10 BLISTER PACK in 1 BAG (55154-5652-0) > 1 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2011-04-01 | 0000-00-00 | No | No | Current |