acyclovir
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
- acyclovir
- Generic name
- ACYCLOVIR
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- fdf6b492-a76e-4cea-89a1-a5b19c7938ff
- SPL ID
- ed4f7f52-6254-46ad-8be4-e830705bbcfa
- Version
- 4
- Effective date
- 2024-08-14
- Source export date
- 2026-11-06
- 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/2026-11-06/8ec9b1418c25a8bb472a36e6bc0b2cbabb210d48d5dd734197e022d21529ed58/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 09:14:42
| Harmonized routes |
|---|
| TOPICAL |
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 | 205974 | derived:openfda.application_number |
| application number | ANDA205974 | openfda.application_number | |
| brand name | acyclovir | openfda.brand_name | |
| generic name | ACYCLOVIR | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1371-2 | openfda.package_ndc |
| ndc | package | 70771-1371-1 | openfda.package_ndc |
| ndc | product | 70771-1371 | openfda.product_ndc |
| ndc11 | package | 70771137101 | derived:openfda.package_ndc |
| ndc11 | package | 70771137102 | derived:openfda.package_ndc |
| rxcui | 197312 | openfda.rxcui | |
| spl id | ed4f7f52-6254-46ad-8be4-e830705bbcfa | id | |
| spl set id | fdf6b492-a76e-4cea-89a1-a5b19c7938ff | set_id | |
| unii | X4HES1O11F | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.