NDC 0591-3195 - Metoprolol tartrate
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
- 0591-3195
- Package NDCs from labels
- 0591-3195-26, 0591-3195-78
- Manufacturer
- Watson laboratories, Inc.
- Effective date
- 2006-04-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| METOPROLOL TARTRATE INJECTION USP Rx only | Watson laboratories, Inc. | 2006-04-07 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Metoprolol tartrate | ACTIVE INGREDIENT | W5S57Y3A5L | METOPROLOL TARTRATE (METOPROLOL TARTRATE) INJECTION [WATSON LABORATORIES, INC.] | 1 | |
| Metoprolol | ACTIVE MOIETY | GEB06NHM23 | METOPROLOL TARTRATE (METOPROLOL TARTRATE) INJECTION [WATSON LABORATORIES, INC.] | 1 | |
| Sodium Chloride | INACTIVE INGREDIENT | 451W47IQ8X | METOPROLOL TARTRATE (METOPROLOL TARTRATE) INJECTION [WATSON LABORATORIES, INC.] | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | METOPROLOL TARTRATE (METOPROLOL TARTRATE) INJECTION [WATSON LABORATORIES, INC.] | 1 |
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 |
|---|---|---|---|---|---|---|
| AD674645-D468-4720-B2FF-D47E96C061B3 | AD674645-D468-4720-B2FF-D47E96C061B3 | 2006-04-07 | Warnings, Adverse reactions | AD674645-D468-4720-B2FF-D47E96C061B3 AD674645-D468-4720-B2FF-D47E96C061B3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.