Chlordiazepoxide Hydrochloride
- Product NDC
- 53217-183
- 11-digit product format
- 532170183
- Labeler code
- 53217
- Product ID
- 53217-183_3a6004e6-835b-4a43-b66e-4b58091fb441
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- 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
- 2019-12-31
- 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 |
|---|
| 53217-183-30 | Chlordiazepoxide Hydrochloride | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-183 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 1 package rows | 20170302_de9d6bb4-22a4-4175-ac7c-31b581510240.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-183-30 | 53217018330 | 30 in 1 BOTTLE | Historical |