Chlorpromazine Hydrochloride
- Product NDC
- 50090-2865
- 11-digit product format
- 500902865
- Labeler code
- 50090
- Product ID
- 50090-2865_051b27be-b940-435a-bce8-470a4ca993ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA084114
- Marketing category
- ANDA
- Marketing start
- 2011-08-03
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2865-0 | Chlorpromazine Hydrochloride | 32 in 1 BOTTLE, UNIT-DOSE | TABLET, SUGAR COATED | 32 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2865 | CHLORPROMAZINE HYDROCHLORIDE TABLET, SUGAR COATED [A-S MEDICATION SOLUTIONS] | 17 | Legacy NDC, 1 package rows | 20210302_3b8545ef-312d-4af6-a082-2497b84ff161.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 |
|---|
| 50090-2865-0 | 50090286500 | 32 TABLET, SUGAR COATED in 1 BOTTLE, UNIT-DOSE (50090-2865-0) | 2017-02-14 | 0000-00-00 | No | No | Current |