NDC 52959-839 - Hypertensolol
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
- 52959-839
- Package NDCs from labels
- 52959-839-30
- Manufacturer
- Physician Therapeutics LLC | Emcure Pharmaceuticals Ltd. | H.J. Harkins Company, Inc. | Targeted Medical Pharma, Inc.
- Effective date
- 2011-08-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hypertensolol | Physician Therapeutics LLC | Emcure Pharmaceuticals Ltd. | H.J. Harkins Company, Inc. | Targeted Medical Pharma, Inc. | 2011-08-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52959-839-30 | Hypertensolol | 30 in 1 BOTTLE | TABLET | 30 | 50 mg | 10 |
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.