NDC 70518-4142-01 - Chlorpromazine Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70518-4142
- Requested NDC
- 70518-4142-01
- Package NDCs from labels
- 70518-4142-1, 70518-4142-0, 70518-4142-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-05-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Chlorpromazine Hydrochloride Tablets, USP | REMEDYREPACK INC. | 2026-05-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-4142-0 | Chlorpromazine Hydrochloride | 100 in 1 BOX | TABLET, SUGAR COATED | 100 | 4 | |
| 70518-4142-1 | Chlorpromazine Hydrochloride | 1 in 1 POUCH | TABLET, SUGAR COATED | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-4142 | CHLORPROMAZINE HYDROCHLORIDE TABLET, SUGAR COATED [REMEDYREPACK INC.] | 1 | Current NDC, 2 package rows | 20240718_b8137906-946c-455d-87c0-0e130cd9266f.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.