Chlordiazepoxide Hydrochloride
- Product NDC
- 64725-0159
- 11-digit product format
- 647250159
- Labeler code
- 64725
- Product ID
- 64725-0159_6689dca3-528e-4013-89d5-b42fcca486d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA084769
- Marketing category
- ANDA
- Marketing start
- 1976-07-02
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-0159-1 | Chlordiazepoxide Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0159 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20140901_b1bd1c1a-0b80-4ef0-94e1-c00cc3010601.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0159-1 | 64725015901 | 100 in 1 BOTTLE | Historical |