NDC 51688-6009 - A3736-22
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
- 51688-6009
- Package NDCs from labels
- 51688-6009-2
- Manufacturer
- Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.
- Effective date
- 2011-06-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| A3736-22 - Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc. | Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc. | 2011-06-03 | MEDICAL DEVICE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0409-4713-65 | A3736-22 | 5 mL in 1 AMPULE | INJECTION, SOLUTION | 5 mL | 10 mg in 1mL | 4 |
| 51688-6009-2 | A3736-22 | 1 in 1 PACKAGE, COMBINATION | KIT | 1 | 4 | |
| 51688-6009-2 | A3736-22 | 10 in 1 CASE | KIT | 10 | 4 | |
| 52380-0001-3 | A3736-22 | 9.8 g in 1 PACKET | SOLUTION | 9.8 g | 9.8 g in 100g | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51688-6009 | (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 4 | 4 package rows | 20110607_c38ce5e9-5b1c-4ec8-bf85-12199a84f5a5.zip |
DailyMed Socrata Ingredients#
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.
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| Lights Povidone Iodine Prep Pad | POVIDONE-IODINE | Lights Medical Manufacture Co., Ltd. | e561332d-e419-43db-a68e-0c0d49b01c9a | 2026-01-21 | Warnings | 85H0HZU99M |
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| Lights Povidone Iodine Solution | POVIDONE-IODINE | Lights Medical Manufacture Co., Ltd. | 7d4a92be-0601-4256-bc5b-bc1b07d97bb7 | 2026-01-21 | Warnings | 312564 85H0HZU99M |
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| Betadine Solution | POVIDONE-IODINE | Atlantis Consumer Healthcare, Inc. | 1b1e224c-8c00-46ea-9bdd-020a9b45321d | 2026-01-21 | Warnings | 312564 85H0HZU99M |
| INSULIN DILUTING MEDIUM FOR Kirsty | WATER | Biocon Biologics Inc. | 3db1d482-7e1f-aec6-79ef-3f305b4d8277 | 2026-01-20 | Warnings, Adverse reactions | 059QF0KO0R |
| Maokang Povidone-Iodine Scrub | POVIDONE-IODINE | Changzhou Maokang Medical Products Co., Ltd | 5f945e64-aee7-4b68-ad8b-9c8d4875842a | 2026-01-20 | Warnings | 85H0HZU99M |
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| Equate Comfort Flow Sinus wash | SINUS WASH | WALMART INC | 9e911eef-ca99-9902-e053-2a95a90aab0e | 2026-01-19 | Warnings | 451W47IQ8X |
| EQUATE PREMIUM SALINE | SODIUM CHLORIDE 0.65% | Walmart Stores, Inc. | 1e17f022-f513-140d-e063-6394a90a379e | 2026-01-19 | Warnings | 451W47IQ8X |
| Sodium chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | d98bf9f7-30ec-4927-a577-cabad192cb18 | 2026-01-19 | Warnings, Adverse reactions | 451W47IQ8X |
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| Sodium Chloride Hypertonicity | SODIUM CHLORIDE | CVS Pharmacy | 9245d842-7f78-42d8-83ba-8eb9ec8dbc0d | 2026-01-15 | Warnings | 451W47IQ8X |
| Sodium Chloride Hypertonicity | SODIUM CHLORIDE | CVS PHARMACY | d5cc6cd1-ddf8-4f5b-a021-204cdda0db94 | 2026-01-15 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.