NDC 71807-011 - ReadyfusOR Ropivacaine Fixed Rate Delivery System
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
- 71807-011
- Package NDCs from labels
- 71807-011-01
- Manufacturer
- BioQ Pharma Incorporated | Holopack Verpackungstechnik (DE) | Steris AST (Frmrly Synergy San Diego) | Steris AST (Frmrly Synergy Daventry ) | A&M Stabtest (Mainz, DE) | Pioneer Agro Industries
- Effective date
- 2018-06-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ropivacaine | BioQ Pharma Incorporated | Holopack Verpackungstechnik (DE) | Steris AST (Frmrly Synergy San Diego) | Steris AST (Frmrly Synergy Daventry ) | A&M Stabtest (Mainz, DE) | Pioneer Agro Industries | 2018-06-22 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71807-011-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-255a-f424-e053-dadaa90a57ce | Ropivacaine |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71807-011-01 | ReadyfusOR RopivacaineFixed Rate Delivery System | 250 mL in 1 BOTTLE, DISPENSING | INJECTION, SOLUTION | 250 | 1 | |
| 71807-011-01 | ReadyfusOR RopivacaineFixed Rate Delivery System | 1 in 1 BOX | INJECTION, SOLUTION | 1 | 1 |
DailyMed Dashboard NDC Coverage#
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 Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| Sodium Chloride | SODIUM CHLORIDE | Baxter Healthcare Corporation | 2a96096d-43cc-49b7-af53-b53c17f41001 | 2014-07-25 | Warnings, Adverse reactions | 451W47IQ8X |
| SODIUM CHLORIDE | SODIUM CHLORIDE | Baxter Healthcare Corporation | b3b4b176-41f0-4ca8-90d4-3fba5707564a | 2014-02-21 | 451W47IQ8X | |
| TIS-U-SOL | SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE | Baxter Healthcare Corporation | 9da4121f-d62d-4da4-8dfb-0494da16015f | 2014-02-21 | 451W47IQ8X | |
| Ringers | SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, | Baxter Healthcare Corporation | e1953d54-818d-46a6-8532-518ebae6d84e | 2012-06-13 | 451W47IQ8X | |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Baxter Healthcare Corporation | f09f80bf-2f8b-4420-865d-aec2d5e5cd4d | 2012-06-12 | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.