National Council for Prescription Drug Programs indexing - billing unit
- Manufacturer
- National Council for Prescription Drug Programs
- Effective date
- 2013-04-01
- Label type
- Indexing - Billing Unit
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-05 04:05:48
Label at a glance#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49281-752-21 | ML - Milliliter | 49281-752 | fcaf285b-9d80-496f-a1d3-07b4fc0d58c3 | 1 | 2013-04-01 |
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49281-752 | 49281-752-21 |
Purple Book Biologic Products#
| BLA | Proprietary name | Proper name | License type | Status | Latest source |
|---|---|---|---|---|---|
| 103941 | Tubersol | Tuberculin, Purified Protein Derivative | 351(a) | Rx | 2026-09-01 |
Source Document#
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 |
|---|---|---|---|---|---|---|
| TUBERSOL | TUBERCULIN PURIFIED PROTEIN DERIVATIVE | Sanofi Vaccines US Inc. | a4a732e9-b8ee-4e6d-8b9a-6a9d2c36bfcd | 2026-05-01 | Warnings, Adverse reactions | 49281-752-21 49281075221 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.