Amitriptyline 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
- Amitriptyline Hydrochloride
- Generic name
- AMITRIPTYLINE HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 4159b10e-f589-486c-969d-9b4544b098b5
- SPL ID
- 64a2af6e-d243-4263-96f3-4c2b3707bf11
- Version
- 7
- Effective date
- 2025-10-04
- Source export date
- 2026-10-30
- 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/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:40:47
| 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 | 210086 | derived:openfda.application_number |
| application number | ANDA210086 | openfda.application_number | |
| brand name | Amitriptyline Hydrochloride | openfda.brand_name | |
| generic name | AMITRIPTYLINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1174-0 | openfda.package_ndc |
| ndc | package | 70771-1176-0 | openfda.package_ndc |
| ndc | package | 70771-1176-1 | openfda.package_ndc |
| ndc | package | 70771-1173-0 | openfda.package_ndc |
| ndc | package | 70771-1175-1 | openfda.package_ndc |
| ndc | package | 70771-1177-0 | openfda.package_ndc |
| ndc | package | 70771-1178-1 | openfda.package_ndc |
| ndc | package | 70771-1175-0 | openfda.package_ndc |
| ndc | package | 70771-1177-1 | openfda.package_ndc |
| ndc | package | 70771-1173-1 | openfda.package_ndc |
| ndc | package | 70771-1174-1 | openfda.package_ndc |
| ndc | package | 70771-1178-0 | openfda.package_ndc |
| ndc | product | 70771-1178 | openfda.product_ndc |
| ndc | product | 70771-1175 | openfda.product_ndc |
| ndc | product | 70771-1174 | openfda.product_ndc |
| ndc | product | 70771-1177 | openfda.product_ndc |
| ndc | product | 70771-1173 | openfda.product_ndc |
| ndc | product | 70771-1176 | openfda.product_ndc |
| ndc11 | package | 70771117400 | derived:openfda.package_ndc |
| ndc11 | package | 70771117300 | derived:openfda.package_ndc |
| ndc11 | package | 70771117601 | derived:openfda.package_ndc |
| ndc11 | package | 70771117600 | derived:openfda.package_ndc |
| ndc11 | package | 70771117801 | derived:openfda.package_ndc |
| ndc11 | package | 70771117800 | derived:openfda.package_ndc |
| ndc11 | package | 70771117501 | derived:openfda.package_ndc |
| ndc11 | package | 70771117500 | derived:openfda.package_ndc |
| ndc11 | package | 70771117401 | derived:openfda.package_ndc |
| ndc11 | package | 70771117701 | derived:openfda.package_ndc |
| ndc11 | package | 70771117700 | derived:openfda.package_ndc |
| ndc11 | package | 70771117301 | derived:openfda.package_ndc |
| rxcui | 856834 | openfda.rxcui | |
| rxcui | 856853 | openfda.rxcui | |
| rxcui | 856783 | openfda.rxcui | |
| rxcui | 856845 | openfda.rxcui | |
| rxcui | 856773 | openfda.rxcui |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.