NDC 70710-1133-2 - 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
- 70710-1133
- Requested NDC
- 70710-1133-2
- Package NDCs from labels
- 70710-1133-1, 70710-1133-2, 70710-1133-4
- Manufacturer
- Major Pharmaceuticals
- Effective date
- 2025-11-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Chlorpromazine hydrochloride - Major Pharmaceuticals | Major Pharmaceuticals | 2025-11-11 | HUMAN PRESCRIPTION DRUG LABEL |
| chlorproMAZINE Hydrochloride Tablets, USP Rx only | Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Global FZE | Zydus Lifesciences Limited | 2024-08-12 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1133-1 | Chlorpromazine hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 5 | |
| 70710-1133-2 | Chlorpromazine hydrochloride | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 5 | |
| 70710-1133-4 | Chlorpromazine hydrochloride | 10 in 1 CARTON | TABLET, FILM COATED | 10 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1133 | CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED [ZYDUS PHARMACEUTICALS (USA) INC.] | 5 | Current NDC, Legacy NDC, 3 package rows | 20240814_fc2bd95d-a7bc-4ab5-bffa-f5059cb8eb63.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1133-1 | EA - Each | 70710-1133 | bf777046-4b18-480a-b2df-4efef26d0ca5 | 1 | 2020-03-10 |
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 |
|---|---|---|---|---|---|---|
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| 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.