NDC11 10135073301
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 10135-0733-01 | 10135-0733 |
| 10135-0733-1 | 10135-0733 |
| 10135-733-01 | 10135-733 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ATENOLOL AND CHLORTHALIDONE | ATENOLOL AND CHLORTHALIDONE TABLET | MARLEX PHARMACEUTICALS, INC | db22ff31-52f6-9024-e053-2995a90af8b3 | 2025-09-22 | Warnings, Adverse reactions | 10135-733-01 10135-733 10135073301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.