NDC 45802-811-00 - NALOXONE HYDROCHLORIDE
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 45802-811
- Requested NDC
- 45802-811-00
- Package NDCs from labels
- 45802-811-00, 45802-811-84
- Manufacturer
- RedPharm Drug
- Effective date
- 2024-07-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| NALOXONE HYDROCHLORIDE - RedPharm Drug | RedPharm Drug | 2024-07-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Naloxone HCl - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2024-06-27 | HUMAN PRESCRIPTION DRUG LABEL |
| NALOXONE HCl - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-01-28 | HUMAN PRESCRIPTION DRUG LABEL |
| NALOXONE HYDROCHLORIDE - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-01-15 | HUMAN PRESCRIPTION DRUG LABEL |
| NALOXONE HYDROCHLORIDE - A-S Medication Solutions | A-S Medication Solutions | 2023-10-01 | HUMAN PRESCRIPTION DRUG LABEL |
| NALOXONE HYDROCHLORIDE - Padagis Israel Pharmaceuticals Ltd | Padagis Israel Pharmaceuticals Ltd | 2023-07-18 | HUMAN PRESCRIPTION DRUG LABEL |
| NALOXONE HYDROCHLORIDE - Quality Care Products, LLC | Quality Care Products, LLC | 2023-03-03 | HUMAN PRESCRIPTION DRUG LABEL |
| NALOXONE HYDROCHLORIDE - Proficient Rx LP | Proficient Rx LP | 2022-10-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 45802-811-00 | EA - Each | 45802-811 | 2584cf2b-1ccf-4b35-8860-0a02bab3901a | 1 | 2022-07-06 |
| 45802-811-84 | EA - Each | 45802-811 | bd196d34-6b1d-493f-85b8-ffb1be112ee7 | 1 | 2022-07-06 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.