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alcaftadine
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
- alcaftadine
- Generic name
- ALCAFTADINE
- Manufacturer
- Alembic Pharmaceuticals Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 22473109-dc9e-45b6-b188-d7d5773f5a14
- SPL ID
- 64d45e8d-158b-42f2-84aa-14fc849eaf0e
- Version
- 3
- Effective date
- 2024-10-07
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:57:51
| Harmonized routes |
|---|
| OPHTHALMIC |
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 | 209290 | derived:openfda.application_number |
| application number | ANDA209290 | openfda.application_number | |
| brand name | alcaftadine | openfda.brand_name | |
| generic name | ALCAFTADINE | openfda.generic_name | |
| manufacturer name | Alembic Pharmaceuticals Inc. | openfda.manufacturer_name | |
| ndc | package | 62332-147-03 | openfda.package_ndc |
| ndc | product | 62332-147 | openfda.product_ndc |
| ndc11 | package | 62332014703 | derived:openfda.package_ndc |
| rxcui | 1000085 | openfda.rxcui | |
| spl id | 64d45e8d-158b-42f2-84aa-14fc849eaf0e | id | |
| spl set id | 22473109-dc9e-45b6-b188-d7d5773f5a14 | set_id | |
| unii | 7Z8O94ECSX | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.