Diltiazem hydrochloride
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
- Diltiazem hydrochloride
- Generic name
- DILTIAZEM HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8329d0ac-d68c-48d2-9cbc-e1a1b60192d9
- SPL ID
- f63d2c9f-f49a-4b36-b25d-6fbe3ab5577f
- Version
- 1
- Effective date
- 2026-05-01
- 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 02:56:04
| 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 | 219253 | derived:openfda.application_number |
| application number | ANDA219253 | openfda.application_number | |
| brand name | Diltiazem hydrochloride | openfda.brand_name | |
| generic name | DILTIAZEM HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1931-1 | openfda.package_ndc |
| ndc | package | 70771-1929-5 | openfda.package_ndc |
| ndc | package | 70771-1930-5 | openfda.package_ndc |
| ndc | package | 70771-1932-1 | openfda.package_ndc |
| ndc | package | 70771-1931-5 | openfda.package_ndc |
| ndc | package | 70771-1932-5 | openfda.package_ndc |
| ndc | package | 70771-1929-1 | openfda.package_ndc |
| ndc | package | 70771-1930-1 | openfda.package_ndc |
| ndc | product | 70771-1929 | openfda.product_ndc |
| ndc | product | 70771-1930 | openfda.product_ndc |
| ndc | product | 70771-1932 | openfda.product_ndc |
| ndc | product | 70771-1931 | openfda.product_ndc |
| ndc11 | package | 70771193001 | derived:openfda.package_ndc |
| ndc11 | package | 70771192901 | derived:openfda.package_ndc |
| ndc11 | package | 70771193101 | derived:openfda.package_ndc |
| ndc11 | package | 70771193005 | derived:openfda.package_ndc |
| ndc11 | package | 70771193105 | derived:openfda.package_ndc |
| ndc11 | package | 70771193201 | derived:openfda.package_ndc |
| ndc11 | package | 70771193205 | derived:openfda.package_ndc |
| ndc11 | package | 70771192905 | derived:openfda.package_ndc |
| rxcui | 831103 | openfda.rxcui | |
| rxcui | 831102 | openfda.rxcui | |
| rxcui | 831054 | openfda.rxcui | |
| rxcui | 833217 | openfda.rxcui | |
| spl id | f63d2c9f-f49a-4b36-b25d-6fbe3ab5577f | id | |
| spl set id | 8329d0ac-d68c-48d2-9cbc-e1a1b60192d9 | set_id | |
| unii | OLH94387TE | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.