NDC 0591-3178 - Citalopram Hydrobromide
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
- 0591-3178
- Package NDCs from labels
- 0591-3178-01, 0591-3178-05, 0591-3178-44
- Manufacturer
- Contract Pharmacy Services-PA
- Effective date
- 2010-02-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Citalopram Hydrobromide - Contract Pharmacy Services-PA | Contract Pharmacy Services-PA | 2010-02-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Citalopram Hydrobromide - Watson Laboratories, Inc | Watson Laboratories, Inc | 2008-01-17 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0591-3178-01 | Citalopram Hydrobromide | 100 in 1 BOTTLE | TABLET | 100 | 4 | |
| 0591-3178-05 | Citalopram Hydrobromide | 500 in 1 BOTTLE | TABLET | 500 | 4 | |
| 0591-3178-44 | Citalopram Hydrobromide | 100 in 1 BLISTER PACK | TABLET | 100 | 4 |
DailyMed Dashboard NDC Coverage#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.