chlorpromazine hydrochloride
- Product NDC
- 62135-421
- 11-digit product format
- 621350421
- Labeler code
- 62135
- Product ID
- 62135-421_459bb2f6-3a40-6998-e063-6394a90a7e2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- chlorpromazine hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA212630
- Marketing category
- ANDA
- Marketing start
- 2022-02-05
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- chlorpromazine hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLORPROMAZINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9WP59609J6 |
| Rxcui | 991039, 991044, 991188, 991194, 991336 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-421-90 | chlorpromazine hydrochloride | 90 in 1 BOTTLE | TABLET, SUGAR COATED | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-421 | CHLORPROMAZINE HYDROCHLORIDE TABLET, SUGAR COATED [CHARTWELL RX, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241011_e9d6a9e9-ba25-4c25-9b03-25897a3ac5f3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62135-421-90 | 62135042190 | 90 TABLET, SUGAR COATED in 1 BOTTLE (62135-421-90) | 2022-10-20 | 0000-00-00 | No | No | Current |