FDA label 980c0ddb-d9a5-49c1-819b-7b1c4a5fc12e
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
- SPL set ID
- d4eb45a2-e65c-409e-8165-be6dee6c9ed0
- SPL ID
- 980c0ddb-d9a5-49c1-819b-7b1c4a5fc12e
- Version
- 9
- Effective date
- 2023-10-23
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:51:33
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 |
|---|---|---|---|
| spl id | 980c0ddb-d9a5-49c1-819b-7b1c4a5fc12e | id | |
| spl set id | d4eb45a2-e65c-409e-8165-be6dee6c9ed0 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warning for this product
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse reaction DISTRIBUTED BY: FODHOLD U.S.A., LLC LANDOVER, MD 20785 1-877-846-9949
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.