CHLORDIAZEPOXIDE HYDROCHLORIDE
- Product NDC
- 42806-562
- 11-digit product format
- 428060562
- Labeler code
- 42806
- Product ID
- 42806-562_eab706f9-1c3b-4be4-a118-4cfd55ce2c11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Epic Pharma LLC
- Application
- ANDA085472
- Marketing category
- ANDA
- Marketing start
- 2021-05-11
- Substance
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MFM6K1XWDK |
DailyMed Product Concepts#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42806-562-01 | 42806056201 | 100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-562-01) | 2021-05-11 | 0000-00-00 | No | No | Current |