NDC 48951-1022-01 - Agaricus Phosphorus
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
- 48951-1022
- Requested NDC
- 48951-1022-01
- Package NDCs from labels
- 48951-1022-1, 48951-1022-01
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2025-11-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Agaricus Phosphorus | Uriel Pharmacy Inc. | 2025-11-21 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1022-1 | Agaricus Phosphorus | 10 in 1 BOX | LIQUID | 10 | 6 | |
| 48951-1022-1 | Agaricus Phosphorus | 1 mL in 1 AMPULE | LIQUID | 1 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-1022 | AGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20241207_b6431e0b-6d84-423f-a1be-6701aa848f8d.zip |
DailyMed Socrata Ingredients#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.