NDC 47781-103-07 - IBANDRONATE SODIUM
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
- 47781-103
- Requested NDC
- 47781-103-07
- Package NDCs from labels
- 47781-103-07, 47781-103-33, 47781-103-21
- Manufacturer
- Alvogen Inc. | OrBion Pharmaceuticals Private Limited
- Effective date
- 2022-04-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| IBANDRONATE SODIUM - Alvogen Inc. | OrBion Pharmaceuticals Private Limited | Alvogen Inc. | OrBion Pharmaceuticals Private Limited | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 47781-103-07 | EA - Each | 47781-103 | 63617f9a-2422-485a-9fc3-83464af22411 | 1 | 2014-06-03 |
| 47781-103-21 | EA - Each | 47781-103 | c2c0ff18-6099-462a-b143-87c92a17bd41 | 1 | 2021-11-09 |
| 47781-103-33 | EA - Each | 47781-103 | ec3513e1-1dbb-4314-ada7-65417c22047b | 1 | 2014-06-03 |
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.