Chlorpromazine Hydrochloride
- Product NDC
- 53808-1104
- 11-digit product format
- 538081104
- Labeler code
- 53808
- Product ID
- 53808-1104_adfb5deb-ddea-4a7d-8762-0c66b17f08b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA084113
- Marketing category
- ANDA
- Marketing start
- 2018-01-03
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 53808-1104-1 | Chlorpromazine Hydrochloride | 30 in 1 BLISTER PACK | TABLET, SUGAR COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1104 | CHLORPROMAZINE HYDROCHLORIDE TABLET, SUGAR COATED [DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20190116_1c4d01a3-fbc2-40da-a646-b7f80db541af.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 |
|---|
| 53808-1104-1 | 53808110401 | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (53808-1104-1) | 2018-01-03 | 0000-00-00 | No | No | Current |