Memantine 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
- Memantine hydrochloride
- Generic name
- MEMANTINE HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ec825bef-2313-45c2-8858-b43197680155
- SPL ID
- 900483ef-de89-464c-a324-8bfaa8f137a6
- Version
- 5
- Effective date
- 2024-11-30
- Source export date
- 2026-10-12
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:25:48
| 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 | 203293 | derived:openfda.application_number |
| application number | ANDA203293 | openfda.application_number | |
| brand name | Memantine hydrochloride | openfda.brand_name | |
| generic name | MEMANTINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1323-2 | openfda.package_ndc |
| ndc | package | 70771-1321-2 | openfda.package_ndc |
| ndc | package | 70771-1323-3 | openfda.package_ndc |
| ndc | package | 70771-1322-2 | openfda.package_ndc |
| ndc | package | 70771-1321-3 | openfda.package_ndc |
| ndc | package | 70771-1323-9 | openfda.package_ndc |
| ndc | package | 70771-1324-4 | openfda.package_ndc |
| ndc | package | 70771-1321-9 | openfda.package_ndc |
| ndc | package | 70771-1324-9 | openfda.package_ndc |
| ndc | package | 70771-1322-9 | openfda.package_ndc |
| ndc | package | 70771-1322-3 | openfda.package_ndc |
| ndc | package | 70771-1324-3 | openfda.package_ndc |
| ndc | package | 70771-1323-4 | openfda.package_ndc |
| ndc | package | 70771-1321-4 | openfda.package_ndc |
| ndc | package | 70771-1322-4 | openfda.package_ndc |
| ndc | package | 70771-1324-2 | openfda.package_ndc |
| ndc | product | 70771-1323 | openfda.product_ndc |
| ndc | product | 70771-1321 | openfda.product_ndc |
| ndc | product | 70771-1324 | openfda.product_ndc |
| ndc | product | 70771-1322 | openfda.product_ndc |
| ndc11 | package | 70771132109 | derived:openfda.package_ndc |
| ndc11 | package | 70771132402 | derived:openfda.package_ndc |
| ndc11 | package | 70771132102 | derived:openfda.package_ndc |
| ndc11 | package | 70771132203 | derived:openfda.package_ndc |
| ndc11 | package | 70771132404 | derived:openfda.package_ndc |
| ndc11 | package | 70771132204 | derived:openfda.package_ndc |
| ndc11 | package | 70771132209 | derived:openfda.package_ndc |
| ndc11 | package | 70771132309 | derived:openfda.package_ndc |
| ndc11 | package | 70771132104 | derived:openfda.package_ndc |
| ndc11 | package | 70771132202 | derived:openfda.package_ndc |
| ndc11 | package | 70771132304 | derived:openfda.package_ndc |
| ndc11 | package | 70771132103 | derived:openfda.package_ndc |
| ndc11 | package | 70771132303 | derived:openfda.package_ndc |
| ndc11 | package | 70771132403 | derived:openfda.package_ndc |
| ndc11 | package | 70771132302 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.