Chlordiazepoxide Hydrochloride
- Product NDC
- 51079-374
- 11-digit product format
- 510790374
- Labeler code
- 51079
- Product ID
- 51079-374_e3de72ff-6f11-79cf-e053-2995a90afb35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA084768
- Marketing category
- ANDA
- Marketing start
- 2022-05-26
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51079-374-01 | Chlordiazepoxide Hydrochloride | 1 in 1 BLISTER PACK | CAPSULE | 1 | | 19 |
| 51079-374-20 | Chlordiazepoxide Hydrochloride | 100 in 1 CARTON | CAPSULE | 100 | | 19 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51079-374 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [MYLAN INSTITUTIONAL INC.] | 16 | Legacy NDC, 2 package rows | 20241009_68c7d8a7-08b3-4a1a-acbd-09bbe67b8d4a.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 |
|---|
| 51079-374-01 | 51079037401 | 1 in 1 BLISTER PACK | | | | | | Historical |
| 51079-374-20 | 51079037420 | 100 BLISTER PACK in 1 CARTON (51079-374-20) > 1 CAPSULE in 1 BLISTER PACK (51079-374-01) | 100 blister pack | 1995-12-08 | 2022-02-28 | No | No | Current |