NDC11 70954052210
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 |
|---|---|
| 70954-0522-10 | 70954-0522 |
| 70954-522-10 | 70954-522 |
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 |
|---|---|---|---|---|---|---|
| INZIRQO | HYDROCHLOROTHIAZIDE | ANI Pharmaceuticals, Inc. | 41aaea48-6c1b-42c8-a96f-5923d49dc934 | 2025-12-16 | Warnings, Adverse reactions | 70954-522-10 70954-522 70954052210 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.