CHLORDIAZEPOXIDE
- Product NDC
- 61919-593
- 11-digit product format
- 619190593
- Labeler code
- 61919
- Product ID
- 61919-593_85b6b71f-54fb-8262-e053-2a91aa0a0f89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORDIAZEPOXIDE
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA085475
- Marketing category
- ANDA
- Marketing start
- 2016-03-04
- 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 |
|---|
| 61919-593-30 | CHLORDIAZEPOXIDE | 30 in 1 BOTTLE | CAPSULE, GELATIN COATED | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-593 | CHLORDIAZEPOXIDE CAPSULE, GELATIN COATED [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20190405_2f1d49ad-13cb-2a23-e054-00144ff88e88.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 |
|---|
| 61919-593-30 | 61919059330 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (61919-593-30) | 2019-04-04 | 0000-00-00 | No | No | Current |