warnings
WARNINGS None known.
Kit for the Preparation of Technetium Tc99m Mertiatide
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
- Kit for the Preparation of Technetium Tc99m Mertiatide
- Generic name
- BETIATIDE
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 0ad62039-f848-4f3d-b489-2524e6b6b86e
- SPL ID
- 21ca1be3-2caf-535c-e063-6394a90a18e5
- Version
- 4
- Effective date
- 2024-09-10
- Source export date
- 2026-09-28
- 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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:44:37
| Harmonized routes |
|---|
| INTRAVENOUS |
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 | 208994 | derived:openfda.application_number |
| application number | ANDA208994 | openfda.application_number | |
| brand name | Kit for the Preparation of Technetium Tc99m Mertiatide | openfda.brand_name | |
| generic name | BETIATIDE | openfda.generic_name | |
| manufacturer name | Sun Pharmaceutical Industries, Inc. | openfda.manufacturer_name | |
| ndc | package | 45567-0655-1 | openfda.package_ndc |
| ndc | product | 45567-0655 | openfda.product_ndc |
| ndc11 | package | 45567065501 | derived:openfda.package_ndc |
| spl id | 21ca1be3-2caf-535c-e063-6394a90a18e5 | id | |
| spl set id | 0ad62039-f848-4f3d-b489-2524e6b6b86e | set_id | |
| unii | 9NV2SR34P8 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS The following adverse reactions have been reported: nausea, vomiting, wheezing, dyspnea, itching, rash, tachycardia, hypertension, shaking chills, fever, and seizure.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.