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NDC 50090-2488-00 Sodium Chloride 9 mg/mL Details
Sodium Chloride 9 mg/mL
Sodium Chloride is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is SODIUM CHLORIDE.
Product Information
| NDC | 50090-2488 |
|---|---|
| Product ID | 50090-2488_4886a92e-66c5-4c98-97c0-6deecebdec4e |
| Associated GPIs | 79750010002018 |
| GCN Sequence Number | 001221 |
| GCN Sequence Number Description | 0.9 % sodium chloride VIAL 0.9 % INJECTION |
| HIC3 | C1B |
| HIC3 Description | SODIUM/SALINE PREPARATIONS |
| GCN | 03034 |
| 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 | 9 |
| Active Ingredient Units | mg/mL |
| Substance Name | SODIUM CHLORIDE |
| Labeler Name | A-S Medication Solutions |
| 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 | ANDA |
| Application Number | ANDA088912 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-2488-00 (50090248800)
| NDC Package Code | 50090-2488-0 |
|---|---|
| Billing NDC | 50090248800 |
| Package | 25 VIAL, SINGLE-DOSE in 1 TRAY (50090-2488-0) / 10 mL in 1 VIAL, SINGLE-DOSE |
| Marketing Start Date | 2016-10-12 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |