NDC 54396-110-60 - Oxandrin
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
- 54396-110
- Requested NDC
- 54396-110-60
- Package NDCs from labels
- 54396-110-60
- Manufacturer
- Savient Pharmaceuticals, Inc.
- Effective date
- 2007-04-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Oxandrin®(oxandrolone tablets, USP)CIII | Savient Pharmaceuticals, Inc. | 2007-04-09 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2013-02-13 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54396-110-60 | Oxandrin | 60 in 1 BOTTLE | TABLET | 60 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 54396-110-60 | EA - Each | 54396-110 | 21c8d7f3-5d02-4f66-a2eb-d51c73b7c885 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| oxandrolone | ACTIVE INGREDIENT | 7H6TM3CT4L | OXANDRIN (OXANDROLONE) TABLET [SAVIENT PHARMACEUTICALS, INC.] | 1 | |
| oxandrolone | ACTIVE MOIETY | 7H6TM3CT4L | OXANDRIN (OXANDROLONE) TABLET [SAVIENT PHARMACEUTICALS, INC.] | 1 | |
| cornstarch | INACTIVE INGREDIENT | OXANDRIN (OXANDROLONE) TABLET [SAVIENT PHARMACEUTICALS, INC.] | 1 | ||
| hydroxypropyl methylcellulose | INACTIVE INGREDIENT | OXANDRIN (OXANDROLONE) TABLET [SAVIENT PHARMACEUTICALS, INC.] | 1 | ||
| lactose | INACTIVE INGREDIENT | OXANDRIN (OXANDROLONE) TABLET [SAVIENT PHARMACEUTICALS, INC.] | 1 | ||
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | OXANDRIN (OXANDROLONE) TABLET [SAVIENT PHARMACEUTICALS, INC.] | 1 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 9DAB9B37-DF9A-8541-FDDC-4F82F5F0E3EB | f622616e-4c11-4149-bf00-5ea5ce97800b | 2007-04-09 | Boxed warning, Warnings, Adverse reactions | 9DAB9B37-DF9A-8541-FDDC-4F82F5F0E3EB f622616e-4c11-4149-bf00-5ea5ce97800b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.