Losartan Potassium
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Losartan Potassium
- Generic name
- LOSARTAN POTASSIUM
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9ccd6823-e813-472c-99cd-c6ef25e74bed
- SPL ID
- 36fa833c-716f-4b69-9326-3c54753240dc
- Version
- 12
- Effective date
- 2026-01-12
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:57:28
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 078243 | derived:openfda.application_number |
| application number | ANDA078243 | openfda.application_number | |
| brand name | Losartan Potassium | openfda.brand_name | |
| generic name | LOSARTAN POTASSIUM | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 65841-730-06 | openfda.package_ndc |
| ndc | package | 65841-731-01 | openfda.package_ndc |
| ndc | package | 65841-729-06 | openfda.package_ndc |
| ndc | package | 65841-731-06 | openfda.package_ndc |
| ndc | package | 65841-729-01 | openfda.package_ndc |
| ndc | package | 65841-729-24 | openfda.package_ndc |
| ndc | package | 65841-729-16 | openfda.package_ndc |
| ndc | package | 65841-730-01 | openfda.package_ndc |
| ndc | package | 65841-729-10 | openfda.package_ndc |
| ndc | package | 65841-731-30 | openfda.package_ndc |
| ndc | package | 65841-730-10 | openfda.package_ndc |
| ndc | package | 65841-731-16 | openfda.package_ndc |
| ndc | package | 65841-731-10 | openfda.package_ndc |
| ndc | package | 65841-730-16 | openfda.package_ndc |
| ndc | package | 65841-730-24 | openfda.package_ndc |
| ndc | package | 65841-731-77 | openfda.package_ndc |
| ndc | product | 65841-731 | openfda.product_ndc |
| ndc | product | 65841-730 | openfda.product_ndc |
| ndc | product | 65841-729 | openfda.product_ndc |
| ndc11 | package | 65841073106 | derived:openfda.package_ndc |
| ndc11 | package | 65841072910 | derived:openfda.package_ndc |
| ndc11 | package | 65841073177 | derived:openfda.package_ndc |
| ndc11 | package | 65841073006 | derived:openfda.package_ndc |
| ndc11 | package | 65841073010 | derived:openfda.package_ndc |
| ndc11 | package | 65841073024 | derived:openfda.package_ndc |
| ndc11 | package | 65841073016 | derived:openfda.package_ndc |
| ndc11 | package | 65841072906 | derived:openfda.package_ndc |
| ndc11 | package | 65841072924 | derived:openfda.package_ndc |
| ndc11 | package | 65841073116 | derived:openfda.package_ndc |
| ndc11 | package | 65841073110 | derived:openfda.package_ndc |
| ndc11 | package | 65841073130 | derived:openfda.package_ndc |
| ndc11 | package | 65841073001 | derived:openfda.package_ndc |
| ndc11 | package | 65841072901 | derived:openfda.package_ndc |
| ndc11 | package | 65841073101 | derived:openfda.package_ndc |
| ndc11 | package | 65841072916 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.