Chlordiazepoxide Hydrochloride
- Product NDC
- 67046-935
- 11-digit product format
- 670460935
- Labeler code
- 67046
- Product ID
- 67046-935_58113333-a25f-2cd0-e053-2991aa0a35ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA085475
- Marketing category
- ANDA
- Marketing start
- 2010-05-15
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-935-30 | Chlordiazepoxide Hydrochloride | 30 in 1 BLISTER PACK | CAPSULE, GELATIN COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-935 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE, GELATIN COATED [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20170915_58113333-a25e-2cd0-e053-2991aa0a35ef.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67046-935-30 | 67046093530 | 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (67046-935-30) | 2017-08-31 | 0000-00-00 | No | No | Current |