NDC 71474-303-50 - keramatrix
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
- 71474-303
- Requested NDC
- 71474-303-50
- Package NDCs from labels
- 71474-303-01, 71474-303-50, 71474-303-10, 71474-303-05, 71474-303-55, 71474-303-51
- Manufacturer
- Molecular Biologicals, LLC
- Effective date
- 2019-03-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| keramatrix - Molecular Biologicals, LLC | Molecular Biologicals, LLC | 2019-03-18 | PRESCRIPTION MEDICAL DEVICE LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71474-303-01 | keramatrix | 1 in 1 POUCH | NOT APPLICABLE | 1 | 3 | |
| 71474-303-01 | keramatrix | 1 in 1 PACKAGE | NOT APPLICABLE | 1 | 3 | |
| 71474-303-05 | keramatrix | 1 in 1 POUCH | NOT APPLICABLE | 1 | 3 | |
| 71474-303-05 | keramatrix | 1 in 1 PACKAGE | NOT APPLICABLE | 1 | 3 | |
| 71474-303-10 | keramatrix | 10 in 1 PACKAGE | NOT APPLICABLE | 10 | 3 | |
| 71474-303-10 | keramatrix | 10 in 1 BOX | NOT APPLICABLE | 10 | 3 | |
| 71474-303-50 | keramatrix | 5 in 1 BOX | NOT APPLICABLE | 5 | 3 | |
| 71474-303-50 | keramatrix | 5 in 1 PACKAGE | NOT APPLICABLE | 5 | 3 | |
| 71474-303-51 | keramatrix | 10 in 1 BOX | NOT APPLICABLE | 10 | 3 | |
| 71474-303-51 | keramatrix | 10 in 1 PACKAGE | NOT APPLICABLE | 10 | 3 | |
| 71474-303-55 | keramatrix | 5 in 1 PACKAGE | NOT APPLICABLE | 5 | 3 | |
| 71474-303-55 | keramatrix | 5 in 1 BOX | NOT APPLICABLE | 5 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71474-303-01 | EA - Each | 71474-303 | 657fb0ba-09f4-4941-95bc-ee18139ad11a | 1 | 2017-08-11 |
| 71474-303-05 | EA - Each | 71474-303 | ea015f6e-0fd9-46f1-bc25-162d33d45d39 | 1 | 2017-08-11 |
| 71474-303-10 | EA - Each | 71474-303 | 58674a60-8489-4e25-b8d0-ef077d9d2281 | 1 | 2017-08-11 |
| 71474-303-50 | EA - Each | 71474-303 | 52fbb997-6d15-43fc-94d0-8d28bfa02b6b | 1 | 2017-08-11 |
| 71474-303-51 | EA - Each | 71474-303 | f1efb25a-a659-4ffa-96ce-0c91e4d01545 | 1 | 2017-08-11 |
| 71474-303-55 | EA - Each | 71474-303 | f759cf5d-a717-429e-9b4e-ffd97c8ca4b9 | 1 | 2017-08-11 |
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 |
|---|---|---|---|---|---|---|
| Quantum Harmony | BLATTA AMERICANA, CEREBRUM SUIS, CACAO, COLUMBUS PALUMBA, HEART (SUIS), DIOSPYROS KAKI, FORMICA RUFA, HYPOTHALAMUS SUIS, HYPOPHYSIS SUIS, PALOONDO, NPY (NEUROPEPTIDE Y), SEROTONIN (HYDROCHLORIDE), SILICEA, SULPHUR, VERATRUM ALBUM, SALIX VITELLINA, FLOS | Deseret Biologicals, Inc. | 1742ac50-ec6e-4261-a0b8-791b893742ef | 2026-02-25 | Warnings | G46579QK1M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.