NDC 0641-6217-01 - ROBAXIN
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
- 0641-6217
- Requested NDC
- 0641-6217-01
- Package NDCs from labels
- 0641-6217-01, 0641-6217-10, 0641-6217-25
- Manufacturer
- Hikma Pharmaceuticals USA Inc.
- Effective date
- 2024-04-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ROBAXIN Injectable (methocarbamol injection, USP) | Hikma Pharmaceuticals USA Inc. | 2024-04-10 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0641-6217-01 | ROBAXIN | 10 mL in 1 VIAL | INJECTION | 10 | 7 | |
| 0641-6217-10 | ROBAXIN | 10 in 1 CARTON | INJECTION | 10 | 7 | |
| 0641-6217-25 | ROBAXIN | 25 in 1 CARTON | INJECTION | 25 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0641-6217-01 | ML - Milliliter | 0641-6217 | 2438936d-92e9-4049-b7e6-e5cd29d24ec4 | 1 | 2018-04-19 |
| 0641-6217-10 | ML - Milliliter | 0641-6217 | 6b59dbca-486a-44fe-873d-0de61865480a | 1 | 2024-05-16 |
| 0641-6217-25 | ML - Milliliter | 0641-6217 | 62677966-065d-4f14-b2de-140ea2a4e67e | 1 | 2018-04-19 |
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 |
| 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.