Chlordiazepoxide Hydrochloride
- Product NDC
- 67046-0910
- 11-digit product format
- 670460910
- Labeler code
- 67046
- Product ID
- 67046-0910_51126cec-445d-7457-e063-6394a90ac87e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Couper LLC
- Application
- ANDA084769
- Marketing category
- ANDA
- Marketing start
- 2026-05-05
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Chlordiazepoxide Hydrochloride
- Listing expiration
- 2027-12-31
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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-0910-3 | Chlordiazepoxide Hydrochloride | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-0910-3 | 67046091003 | 30 CAPSULE in 1 BLISTER PACK (67046-0910-3) | 30 capsule | 2026-05-05 | No | No | Historical |