Chlordiazepoxide Hydrochloride
- Product NDC
- 43353-969
- 11-digit product format
- 433530969
- Labeler code
- 43353
- Product ID
- 43353-969_e0078bdb-6976-4f1a-b2e8-c9c0fbc8360e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA085472
- Marketing category
- ANDA
- Marketing start
- 2002-09-26
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43353-969 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE, GELATIN COATED [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 3 | Legacy NDC | 20171128_a6a63bd7-adcb-4909-84b4-30c0dc1d76f2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-969-53 | 43353096953 | 60 CAPSULE, GELATIN COATED in 1 BOTTLE (43353-969-53) | 2014-10-04 | 0000-00-00 | No | No | Current |