Chlordiazepoxide Hydrochloride
- Product NDC
- 68071-5171
- 11-digit product format
- 680715171
- Labeler code
- 68071
- Product ID
- 68071-5171_1b567b38-ffc3-11d0-e063-6394a90a6c7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA084769
- Marketing category
- ANDA
- Marketing start
- 1976-07-01
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Chlordiazepoxide Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLORDIAZEPOXIDE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MFM6K1XWDK |
| Rxcui | 905495 |
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 |
|---|
| 68071-5171-3 | Chlordiazepoxide Hydrochloride | 30 in 1 BOTTLE | CAPSULE | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-5171 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [NUCARE PHARMACEUTICALS,INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240622_9e64d2d8-b12c-5639-e053-2a95a90aab80.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 |
|---|
| 68071-5171-3 | 68071517103 | 30 CAPSULE in 1 BOTTLE (68071-5171-3) | 30 capsule | 2020-02-12 | 0000-00-00 | No | No | Current |