NDC 48951-8084-01 - Pulmo Bryonia
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
- 48951-8084
- Requested NDC
- 48951-8084-01
- Package NDCs from labels
- 48951-8084-1, 48951-8084-01
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2025-08-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pulmo Bryonia | Uriel Pharmacy Inc. | 2025-08-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-8084-1 | Pulmo Bryonia | 1 mL in 1 AMPULE | LIQUID | 1 | 4 | |
| 48951-8084-1 | Pulmo Bryonia | 10 in 1 BOX | LIQUID | 10 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-8084 | PULMO BRYONIA LIQUID [URIEL PHARMACY INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20180525_a6752cc7-ff8c-4c34-a0a9-0658a915c8cc.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.