Indomethacin
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
- Indomethacin
- Generic name
- INDOMETHACIN
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c6ca86fb-df23-42c1-9d29-f15312faf60c
- SPL ID
- 6d0a7b56-9d42-4fe8-9166-408267ded644
- Version
- 1
- Effective date
- 2023-08-03
- Source export date
- 2026-10-12
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:26:47
| Harmonized routes |
|---|
| RECTAL |
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 | 216184 | derived:openfda.application_number |
| application number | ANDA216184 | openfda.application_number | |
| brand name | Indomethacin | openfda.brand_name | |
| generic name | INDOMETHACIN | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1766-6 | openfda.package_ndc |
| ndc | package | 70771-1766-7 | openfda.package_ndc |
| ndc | product | 70771-1766 | openfda.product_ndc |
| ndc11 | package | 70771176606 | derived:openfda.package_ndc |
| ndc11 | package | 70771176607 | derived:openfda.package_ndc |
| rxcui | 197819 | openfda.rxcui | |
| spl id | 6d0a7b56-9d42-4fe8-9166-408267ded644 | id | |
| spl set id | c6ca86fb-df23-42c1-9d29-f15312faf60c | set_id | |
| unii | XXE1CET956 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.