Chlorpromazine Hydrochloride
- Product NDC
- 0832-6017
- 11-digit product format
- 008326017
- Labeler code
- 0832
- Product ID
- 0832-6017_787f32b3-e4f6-424d-a2c0-d249b5bbcd93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA083386
- Marketing category
- ANDA
- Marketing start
- 2011-08-08
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Chlorpromazine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLORPROMAZINE HYDROCHLORIDE | 10 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 |
|---|
| 0832-6017-00 | Chlorpromazine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0832-6017 | CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED [UPSHER-SMITH LABORATORIES, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230531_5ae79c1e-f523-4358-9f8b-7382a03d59bc.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 |
|---|
| 0832-6017-00 | 00832601700 | 100 TABLET, FILM COATED in 1 BOTTLE (0832-6017-00) | 2021-08-06 | 0000-00-00 | No | No | Current |