Chlorpromazine Hydrochloride
- Product NDC
- 50090-6029
- 11-digit product format
- 500906029
- Labeler code
- 50090
- Product ID
- 50090-6029_fab2d23a-6ab5-476f-9514-ddfcbf19dfec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, FILM 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
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50090-6029-0 | Chlorpromazine Hydrochloride | 32 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 32 | | 8 |
| 50090-6029-0 | Chlorpromazine Hydrochloride | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6029 | CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC, 2 package rows | 20220710_445baba1-acd8-4010-a8a3-e83e8811ef3f.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 |
|---|
| 50090-6029-0 | 50090602900 | 32 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-6029-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 32 blister pack | 2022-07-05 | 0000-00-00 | No | No | Current |