NDC 51672-1315-06 - Mometasone Furoate
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
- 51672-1315
- Requested NDC
- 51672-1315-06
- Package NDCs from labels
- 51672-1315-1, 51672-1315-6, 51672-1315-06
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2025-07-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PHOSPHORIC ACID - Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-07-07 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-1315-1 | Mometasone Furoate | 15 g in 1 TUBE | CREAM | 15 | 6 | |
| 51672-1315-1 | Mometasone Furoate | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-1315-6 | Mometasone Furoate | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-1315-6 | Mometasone Furoate | 45 g in 1 TUBE | CREAM | 45 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-1315 | MOMETASONE FUROATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] | 5 | Current NDC, Legacy NDC, 4 package rows | 20210211_ce61920d-65df-4423-925d-091e624ea32e.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.