Plasma-Lyte 148 (pH 7.4)
- Product NDC
- 0338-9593
- 11-digit product format
- 003389593
- Labeler code
- 0338
- Product ID
- 0338-9593_0fe5a11d-9640-4645-8d45-488a04ea6550
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, Magnesium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start
- 2024-11-08
- Substance
- MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
- Active strength
- 30; 37; 368; 526; 502 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Plasma-Lyte 148 (pH 7.4)
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MAGNESIUM CHLORIDE | 30 mg/100mL |
| POTASSIUM CHLORIDE | 37 mg/100mL |
| SODIUM ACETATE | 368 mg/100mL |
| SODIUM CHLORIDE | 526 mg/100mL |
| SODIUM GLUCONATE | 502 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 02F3473H9O, 660YQ98I10, 4550K0SC9B, 451W47IQ8X, R6Q3791S76 |
| Rxcui | 801109, 801357 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0338-9593-01 | Plasma-Lyte 148 (pH 7.4) | 1000 mL in 1 BAG | INJECTION, SOLUTION | 1000 | | 2 |
| 0338-9593-10 | Plasma-Lyte 148 (pH 7.4) | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0338-9593 | PLASMA-LYTE 148 (PH 7.4) (SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] | 1 | Current NDC, 2 package rows | 20241109_fe935c8d-f42d-42e4-8665-0dc66829f231.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0338-9593-01 | 00338959301 | 1000 mL in 1 BAG | 1000 ml | | | | Historical |
| 0338-9593-10 | 00338959310 | 10 BAG in 1 CARTON (0338-9593-10) / 1000 mL in 1 BAG (0338-9593-01) | 10 bag | 2024-11-08 | No | No | Historical |