Chlorpromazine Hydrochloride
- Product NDC
- 70518-3590
- 11-digit product format
- 705183590
- Labeler code
- 70518
- Product ID
- 70518-3590_f0d3765e-1580-2b7c-e053-2a95a90a6272
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212996
- Marketing category
- ANDA
- Marketing start
- 2022-12-07
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 50 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3590 | CHLORPROMAZINE HYDROCHLORIDE TABLET, COATED [REMEDYREPACK INC.] | 4 | Legacy NDC | 20241011_ae823f6a-1e97-4af3-8caf-73dc3ea1603e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3590-0 | 70518359000 | 30 TABLET, COATED in 1 BLISTER PACK (70518-3590-0) | 2022-12-07 | 0000-00-00 | No | No | Current |