NDC 17856-1002-01 - Risperidone
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
- 17856-1002
- Requested NDC
- 17856-1002-01
- Package NDCs from labels
- 17856-1002-1, 17856-1002-2, 17856-1002-3, 17856-1002-4, 17856-1002-5, 17856-1002-01
- Manufacturer
- ATLANTIC BIOLOGICALS CORP.
- Effective date
- 2026-07-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SORBITOL SOLUTION - ATLANTIC BIOLOGICALS CORP. | ATLANTIC BIOLOGICALS CORP. | 2026-07-10 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-1002-1 | Risperidone | 120 in 1 BOX, UNIT-DOSE | SOLUTION | 120 | 4 | |
| 17856-1002-1 | Risperidone | 1 mL in 1 SYRINGE | SOLUTION | 1 | 4 | |
| 17856-1002-2 | Risperidone | 1 mL in 1 SYRINGE | SOLUTION | 1 | 4 | |
| 17856-1002-2 | Risperidone | 120 in 1 BOX, UNIT-DOSE | SOLUTION | 120 | 4 | |
| 17856-1002-3 | Risperidone | 120 in 1 BOX, UNIT-DOSE | SOLUTION | 120 | 4 | |
| 17856-1002-3 | Risperidone | 2 mL in 1 SYRINGE | SOLUTION | 2 | 4 | |
| 17856-1002-4 | Risperidone | 120 in 1 BOX, UNIT-DOSE | SOLUTION | 120 | 4 | |
| 17856-1002-4 | Risperidone | 3 mL in 1 SYRINGE | SOLUTION | 3 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17856-1002 | RISPERIDONE SOLUTION [ATLANTIC BIOLOGICALS CORP.] | 1 | Current NDC, 8 package rows | 20240921_dc8c6638-f487-49df-a265-78caa93e43d8.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 17856-1002-3 | ML - Milliliter | 17856-1002 | 48537538-588e-4952-846d-489db145bdbf | 1 | 2025-07-08 |
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 |
|---|---|---|---|---|---|---|
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Tox-Chord | ALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUM | Energetix Corp | 6b0d1628-b20d-426e-9c84-5cceadca3f45 | 2016-11-11 | Warnings | 8SKN0B0MIM |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.