NDC 55150-307-01 - ACETAMINOPHEN
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
- 55150-307
- Requested NDC
- 55150-307-01
- Package NDCs from labels
- 55150-307-01, 55150-307-24
- Manufacturer
- HF Acquisition Co LLC, DBA HealthFirst
- Effective date
- 2026-09-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ACETAMINOPHEN - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2026-09-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Acetaminophen - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-08-28 | HUMAN PRESCRIPTION DRUG LABEL |
| Acetaminophen - Eugia US LLC | Eugia Pharma Specialities Limited | Eugia US LLC | Eugia Pharma Specialities Limited | 2023-08-03 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55150-307-01 | Acetaminophen | 100 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 100 | 3 | |
| 55150-307-24 | Acetaminophen | 24 in 1 CARTON | INJECTION, SOLUTION | 24 | 3 |
DailyMed Dashboard NDC Coverage#
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.