Search by Drug Name or NDC
NDC 00264-7707-10 Isolyte S pH 7.4 .03; .037; .00082; .37; .53; .5; .012 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL Details
Isolyte S pH 7.4 .03; .037; .00082; .37; .53; .5; .012 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
Isolyte S pH 7.4 is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by B. Braun Medical Inc.. The primary component is MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC.
Product Information
| NDC | 00264-7707 |
|---|---|
| Product ID | 0264-7707_88c0041b-2b08-4ca1-b733-60f8b5723892 |
| Associated GPIs | 79992001872000 |
| GCN Sequence Number | 001458 |
| GCN Sequence Number Description | electrolyte-S (ph 7.4) IV SOLN INTRAVEN |
| HIC3 | C1W |
| HIC3 Description | ELECTROLYTE MAINTENANCE |
| GCN | 05911 |
| HICL Sequence Number | 000627 |
| HICL Sequence Number Description | ELECTROLYTE-S (PH 7.4) |
| Brand/Generic | Brand |
| Proprietary Name | Isolyte S pH 7.4 |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, and POTASSIUM PHOSPHATE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | .03; .037; .00082; .37; .53; .5; .012 |
| Active Ingredient Units | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Substance Name | MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC |
| Labeler Name | B. Braun Medical Inc. |
| Pharmaceutical Class | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased La |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA019696 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00264-7707-10 (00264770710)
| NDC Package Code | 0264-7707-10 |
|---|---|
| Billing NDC | 00264770710 |
| Package | 24 CONTAINER in 1 CASE (0264-7707-10) / 500 mL in 1 CONTAINER |
| Marketing Start Date | 1989-09-29 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |