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NDC 00990-7984-13 Sodium Chloride 900 mg/100mL Details
Sodium Chloride 900 mg/100mL
Sodium Chloride is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ICU Medical Inc.. The primary component is SODIUM CHLORIDE.
Product Information
| NDC | 00990-7984 |
|---|---|
| Product ID | 0990-7984_4e92e246-09fd-4167-b5d6-517df56a46f2 |
| Associated GPIs | 79750010002021 |
| GCN Sequence Number | 001210 |
| GCN Sequence Number Description | 0.9 % sodium chloride IV SOLN 0.9 % INTRAVEN |
| HIC3 | C1B |
| HIC3 Description | SODIUM/SALINE PREPARATIONS |
| GCN | 02962 |
| 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, SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 900 |
| Active Ingredient Units | mg/100mL |
| Substance Name | SODIUM CHLORIDE |
| Labeler Name | ICU Medical Inc. |
| 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 | NDA016366 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00990-7984-13 (00990798413)
| NDC Package Code | 0990-7984-13 |
|---|---|
| Billing NDC | 00990798413 |
| Package | 48 POUCH in 1 CASE (0990-7984-13) / 1 BAG in 1 POUCH / 50 mL in 1 BAG |
| Marketing Start Date | 2019-05-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |