Emtricitabine and tenofovir disoproxil fumarate
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
- Emtricitabine and tenofovir disoproxil fumarate
- Generic name
- EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- a0ee89b6-72c3-4b99-8d1c-d7473f1d5ef3
- SPL ID
- 8fb1b15c-e324-4410-9a1b-2b3a2ffee3f6
- Version
- 6
- Effective date
- 2024-11-28
- 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 05:48:31
| 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 | 212689 | derived:openfda.application_number |
| application number | ANDA212689 | openfda.application_number | |
| brand name | Emtricitabine and tenofovir disoproxil fumarate | openfda.brand_name | |
| generic name | EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1621-2 | openfda.package_ndc |
| ndc | package | 70771-1620-9 | openfda.package_ndc |
| ndc | package | 70771-1621-4 | openfda.package_ndc |
| ndc | package | 70771-1620-3 | openfda.package_ndc |
| ndc | package | 70771-1620-4 | openfda.package_ndc |
| ndc | package | 70771-1622-9 | openfda.package_ndc |
| ndc | package | 70771-1622-2 | openfda.package_ndc |
| ndc | package | 70771-1709-9 | openfda.package_ndc |
| ndc | package | 70771-1709-4 | openfda.package_ndc |
| ndc | package | 70771-1709-3 | openfda.package_ndc |
| ndc | package | 70771-1621-9 | openfda.package_ndc |
| ndc | package | 70771-1622-3 | openfda.package_ndc |
| ndc | package | 70771-1621-3 | openfda.package_ndc |
| ndc | package | 70771-1622-4 | openfda.package_ndc |
| ndc | package | 70771-1620-2 | openfda.package_ndc |
| ndc | package | 70771-1709-2 | openfda.package_ndc |
| ndc | product | 70771-1620 | openfda.product_ndc |
| ndc | product | 70771-1709 | openfda.product_ndc |
| ndc | product | 70771-1622 | openfda.product_ndc |
| ndc | product | 70771-1621 | openfda.product_ndc |
| ndc11 | package | 70771162202 | derived:openfda.package_ndc |
| ndc11 | package | 70771162004 | derived:openfda.package_ndc |
| ndc11 | package | 70771162003 | derived:openfda.package_ndc |
| ndc11 | package | 70771170903 | derived:openfda.package_ndc |
| ndc11 | package | 70771170904 | derived:openfda.package_ndc |
| ndc11 | package | 70771162203 | derived:openfda.package_ndc |
| ndc11 | package | 70771162102 | derived:openfda.package_ndc |
| ndc11 | package | 70771162209 | derived:openfda.package_ndc |
| ndc11 | package | 70771170909 | derived:openfda.package_ndc |
| ndc11 | package | 70771162103 | derived:openfda.package_ndc |
| ndc11 | package | 70771162009 | derived:openfda.package_ndc |
| ndc11 | package | 70771162002 | derived:openfda.package_ndc |
| ndc11 | package | 70771162204 | derived:openfda.package_ndc |
| ndc11 | package | 70771162104 | derived:openfda.package_ndc |
| ndc11 | package | 70771162109 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.