Chlordiazepoxide Hydrochloride
- Product NDC
- 17856-0164
- 11-digit product format
- 178560164
- Labeler code
- 17856
- Product ID
- 17856-0164_6e9b1118-f258-4408-9f00-4bda8c56a07d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- 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
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 |
|---|
| 17856-0164-1 | 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 |
|---|
| 17856-0164 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [ATLANTIC BIOLOGICALS CORP.] | 1 | Legacy NDC, 1 package rows | 20210406_44a0c8b0-5a9f-4014-a972-e9d0f51747d3.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 |
|---|
| 17856-0164-1 | 17856016401 | 30 CAPSULE in 1 BLISTER PACK (17856-0164-1) | 30 capsule | 2021-04-05 | 0000-00-00 | No | No | Current |