NDC11 50066020201
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 |
|---|---|
| 50066-0202-01 | 50066-0202 |
| 50066-0202-1 | 50066-0202 |
| 50066-202-01 | 50066-202 |
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 |
|---|---|---|---|---|---|---|
| TRIPLE ANTIBIOTIC PLUS PAIN RELIEF | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | GENOMMA LAB USA, INC. | 506fcda5-df44-49c8-8dbd-cab7434b06b2 | 2025-07-02 | Warnings | 50066-202-01 50066-202 50066020201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.