NDC 0832-0302-89 - 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
- 0832-0302
- Requested NDC
- 0832-0302-89
- Package NDCs from labels
- 0832-0302-00, 0832-0302-10, 0832-0302-89, 0832-0302-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2023-08-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ChlorproMAZINE Hydrochloride Tablets, USP | REMEDYREPACK INC. | 2023-08-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Acacia - Upsher-Smith Laboratories, Inc. | Upsher-Smith Laboratories, LLC | Upsher-Smith Laboratories, Inc. | Upsher-Smith Laboratories, LLC | 2023-03-31 | HUMAN PRESCRIPTION DRUG LABEL |
| ChlorproMAZINE Hydrochloride Tablets, USP | REMEDYREPACK INC. | 2021-01-14 | HUMAN PRESCRIPTION DRUG LABEL |
| ChlorproMAZINE Hydrochloride Tablets, USP | Mylan Institutional Inc. | 2019-12-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Chlorpromazine Hydrochloride - DOH CENTRAL PHARMACY | DOH CENTRAL PHARMACY | 2019-01-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Chlorpromazine Hydrochloride - Carilion Materials Management | Carilion Materials Management | 2018-02-06 | HUMAN PRESCRIPTION DRUG LABEL |
| chlorpromazine hydrochloride - State of Florida DOH Central Pharmacy | State of Florida DOH Central Pharmacy | 2010-05-21 | HUMAN PRESCRIPTION DRUG LABEL |
| chlorpromazine hydrochloride - Contract Pharmacy Services-PA | Contract Pharmacy Services-PA | 2010-02-25 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0832-0302-00 | EA - Each | 0832-0302 | b203caac-7fab-44ff-b6cd-86169c2a6996 | 1 | 2012-07-24 |
| 0832-0302-10 | EA - Each | 0832-0302 | fcab8c65-b989-480a-888e-90c30f0d5b8b | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.