Chlordiazepoxide Hydrochloride
- Product NDC
- 62135-222
- 11-digit product format
- 621350222
- Labeler code
- 62135
- Product ID
- 62135-222_459b61a4-0838-cea1-e063-6394a90af06c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlordiazepoxide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA084679
- Marketing category
- ANDA
- Marketing start
- 1976-06-15
- 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 | 905369, 905495, 905516 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-222-60 | Chlordiazepoxide Hydrochloride | 60 in 1 BOTTLE | CAPSULE | 60 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-222 | CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [CHARTWELL RX, LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241011_dd5f82b0-5a56-4728-941a-c8c2a0d51cc4.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 |
|---|
| 62135-222-60 | 62135022260 | 60 CAPSULE in 1 BOTTLE (62135-222-60) | 60 capsule | 2022-04-18 | 0000-00-00 | No | No | Current |