Sodium chloride is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Sodium Chloride.
| Product ID | 63323-623_2a168686-9085-41e5-b098-23868e649911 |
| NDC | 63323-623 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Sodium chloride |
| Generic Name | Sodium Chloride |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2017-09-19 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA207310 |
| Labeler Name | Fresenius Kabi USA, LLC |
| Substance Name | SODIUM CHLORIDE |
| Active Ingredient Strength | 9 mg/mL |
| Pharm Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2017-09-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug for use in drug shor |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-02-18 |
| Marketing End Date | 2014-06-24 |
| Marketing Category | ANDA |
| Application Number | ANDA207310 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-09-19 |
| Marketing Category | Unapproved drug for use in drug shor |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-02-18 |
| Marketing End Date | 2016-11-14 |
| Marketing Category | Unapproved drug for use in drug shor |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-02-18 |
| Marketing End Date | 2016-04-08 |
| Marketing Category | ANDA |
| Application Number | ANDA207310 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-09-19 |
| Marketing Category | Unapproved drug for use in drug shor |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-02-18 |
| Marketing End Date | 2014-06-24 |
| Marketing Category | Unapproved drug for use in drug shor |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-02-18 |
| Marketing End Date | 2015-02-05 |
| Marketing Category | ANDA |
| Application Number | ANDA207310 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-09-19 |
| Marketing Category | Unapproved drug for use in drug shor |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-02-18 |
| Marketing End Date | 2014-06-24 |
| Marketing Category | ANDA |
| Application Number | ANDA207310 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-09-19 |
| Marketing Category | Unapproved drug for use in drug shor |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2014-02-18 |
| Marketing End Date | 2014-06-24 |
| Marketing Category | ANDA |
| Application Number | ANDA207310 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-09-19 |
| Ingredient | Strength |
|---|---|
| SODIUM CHLORIDE | 9 mg/mL |
| SPL SET ID: | c1e52670-c85e-4f19-a2e9-bf9abd7c3727 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0019-1188 | SODIUM CHLORIDE | sodium chloride |
| 0264-1800 | Sodium Chloride | Sodium Chloride |
| 0264-2201 | Sodium Chloride | Sodium Chloride |
| 0264-5802 | Sodium Chloride | SODIUM CHLORIDE |
| 0264-5804 | Sodium Chloride | SODIUM CHLORIDE |
| 0264-7800 | Sodium Chloride | Sodium Chloride |
| 0264-7802 | Sodium Chloride | SODIUM CHLORIDE |
| 0264-7805 | Sodium Chloride | Sodium Chloride |
| 0264-7806 | Sodium Chloride | Sodium Chloride |
| 0264-9375 | Sodium Chloride | Sodium Chloride |
| 0264-9999 | Sodium Chloride | Sodium Chloride |
| 0338-0043 | Sodium Chloride | Sodium Chloride |
| 0409-4888 | Sodium Chloride | Sodium Chloride |
| 0409-6138 | Sodium Chloride | Sodium Chloride |
| 0409-6660 | Sodium Chloride | Sodium Chloride |
| 0409-7101 | Sodium Chloride | Sodium Chloride |
| 0409-7138 | Sodium Chloride | Sodium Chloride |
| 0409-7132 | Sodium Chloride | Sodium Chloride |
| 0409-7972 | Sodium Chloride | Sodium Chloride |
| 0409-7983 | Sodium Chloride | Sodium Chloride |
| 0409-7984 | Sodium Chloride | Sodium Chloride |
| 0409-7730 | Sodium Chloride | Sodium Chloride |
| 0409-7985 | Sodium Chloride | Sodium Chloride |
| 0487-9301 | Sodium Chloride | Sodium Chloride |
| 0517-2810 | Sodium Chloride | Sodium Chloride |
| 70518-1425 | Sodium Chloride | Sodium Chloride |
| 76297-001 | Sodium Chloride | Sodium Chloride |
| 0641-1512 | Sodium Chloride | Sodium Chloride |
| 0641-0497 | Sodium Chloride | Sodium Chloride |
| 0641-6144 | Sodium Chloride | Sodium Chloride |
| 0990-7984 | Sodium Chloride | Sodium Chloride |
| 11822-5458 | Sodium Chloride | Sodium Chloride |
| 17238-625 | Sodium Chloride | Sodium Chloride |
| 17271-701 | Sodium chloride | Sodium chloride |
| 17478-622 | Sodium Chloride | Sodium Chloride |
| 17478-623 | Sodium Chloride | Sodium Chloride |
| 46163-300 | Sodium Chloride | Sodium Chloride |
| 49230-300 | Sodium Chloride | Sodium Chloride |
| 50090-2488 | Sodium Chloride | Sodium Chloride |
| 51662-1342 | SODIUM CHLORIDE | SODIUM CHLORIDE |
| 51662-1258 | SODIUM CHLORIDE | SODIUM CHLORIDE |
| 51662-1318 | SODIUM CHLORIDE | SODIUM CHLORIDE |
| 52584-025 | Sodium Chloride | Sodium Chloride |
| 52584-888 | Sodium Chloride | Sodium Chloride |
| 55154-6979 | Sodium Chloride | Sodium Chloride |
| 55154-0126 | Sodium Chloride | Sodium Chloride |
| 0220-0432 | Aqua marina | SODIUM CHLORIDE |
| 0220-3582 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3583 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3586 | Natrum muriaticum | SODIUM CHLORIDE |