NDC 0009-0036 - Halotestin
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
- 0009-0036
- Package NDCs from labels
- 0009-0036-03, 0009-0036-04
- Manufacturer
- Pharmacia and Upjohn Company
- Effective date
- 2006-02-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Halotestin - Pharmacia and Upjohn Company | Pharmacia and Upjohn Company | 2006-02-06 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0009-0036-03 | Halotestin | 30 in 1 BOTTLE | TABLET | 30 | 1 | |
| 0009-0036-04 | Halotestin | 100 in 1 BOTTLE | TABLET | 100 | 1 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 98E72B58-1876-5C1E-9132-84C7D64D24EB | 09BAFC2D-1893-4618-86DC-E9403407CD41 | 2006-02-06 | Warnings, Adverse reactions | 98E72B58-1876-5C1E-9132-84C7D64D24EB 09BAFC2D-1893-4618-86DC-E9403407CD41 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.