Chlorpromazine Hydrochloride
- Product NDC
- 51407-435
- 11-digit product format
- 514070435
- Labeler code
- 51407
- Product ID
- 51407-435_45b74177-0987-aecc-e063-6294a90a1625
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA212996
- Marketing category
- ANDA
- Marketing start
- 2021-01-22
- 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 |
|---|
| 51407-435-01 | Chlorpromazine Hydrochloride | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-435 | CHLORPROMAZINE HYDROCHLORIDE TABLET, COATED [GOLDEN STATE MEDICAL SUPPLY, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241019_c212a2a1-323a-8b61-e053-2995a90a5b04.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 |
|---|
| 51407-435-01 | 51407043501 | 100 TABLET, COATED in 1 BOTTLE (51407-435-01) | 2021-02-16 | 0000-00-00 | No | No | Current |