NDC 17856-0620-01 - Baclofen
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
- 17856-0620
- Requested NDC
- 17856-0620-01
- Package NDCs from labels
- 17856-0620-1, 17856-0620-2, 17856-0620-3, 17856-0620-4, 17856-0620-5, 17856-0620-9, 17856-0620-01
- Manufacturer
- Atlantic Biologicals Corp.
- Effective date
- 2026-09-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Baclofen - Atlantic Biologicals Corp. | Atlantic Biologicals Corp. | 2026-09-04 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-0620-1 | Baclofen | 2.5 mL in 1 CUP, UNIT-DOSE | SOLUTION | 2.5 | 2 | |
| 17856-0620-1 | Baclofen | 72 in 1 CASE | SOLUTION | 72 | 2 | |
| 17856-0620-2 | Baclofen | 5 mL in 1 CUP, UNIT-DOSE | SOLUTION | 5 | 2 | |
| 17856-0620-2 | Baclofen | 72 in 1 CASE | SOLUTION | 72 | 2 |
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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| FIND BICHON CLEANSING MASK | GLYCERIN | Pioom Cosmetic Co.,ltd | 50b7db48-7b55-6df4-e054-00144ff88e88 | 2017-05-30 | Warnings | PDC6A3C0OX |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| 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.