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NDC 00338-9159-30 SODIUM CHLORIDE 900 mg/100mL Details
SODIUM CHLORIDE 900 mg/100mL
SODIUM CHLORIDE is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is SODIUM CHLORIDE.
Product Information
| NDC | 00338-9159 |
|---|---|
| Product ID | 0338-9159_616e481c-4910-4f2a-807e-78a41da381d6 |
| Associated GPIs | 79750010002021 |
| GCN Sequence Number | 060476 |
| GCN Sequence Number Description | 0.9 % sodium chloride PGY VL PRT INTRAVEN |
| HIC3 | C1B |
| HIC3 Description | SODIUM/SALINE PREPARATIONS |
| GCN | 26637 |
| HICL Sequence Number | 008255 |
| HICL Sequence Number Description | 0.9 % SODIUM CHLORIDE |
| Brand/Generic | Generic |
| Proprietary Name | SODIUM CHLORIDE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | sodium chloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 900 |
| Active Ingredient Units | mg/100mL |
| Substance Name | SODIUM CHLORIDE |
| Labeler Name | Baxter Healthcare Corporation |
| Pharmaceutical Class | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA020178 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00338-9159-30 (00338915930)
| NDC Package Code | 0338-9159-30 |
|---|---|
| Billing NDC | 00338915930 |
| Package | 100 mL in 1 BAG (0338-9159-30) |
| Marketing Start Date | 2018-09-04 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |