Chlordiazepoxide Hydrochloride
- Product NDC
- 67046-396
- 11-digit product format
- 670460396
- Labeler code
- 67046
- Product ID
- 67046-396_a00dd7f7-7453-13fd-e053-2995a90adc3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Coupler Enterprises Inc.
- Application
- ANDA084768
- Marketing category
- ANDA
- Marketing start
- 2019-11-29
- Marketing end
- 0000-00-00
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 5 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
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 |
|---|
| 67046-396-30 | Chlordiazepoxide Hydrochloride | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-396 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [COUPLER ENTERPRISES INC.] | 1 | Legacy NDC, 1 package rows | 20200305_a00dd797-364f-2d2c-e053-2a95a90a9055.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67046-396-30 | 67046039630 | 30 CAPSULE in 1 BLISTER PACK (67046-396-30) | 30 capsule | 2019-11-29 | 0000-00-00 | No | No | Current |