Search by Drug Name or NDC
NDC 00409-7101-67 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 Hospira, Inc.. The primary component is SODIUM CHLORIDE.
Product Information
| NDC | 00409-7101 |
|---|---|
| Product ID | 0409-7101_bee16468-f227-4840-bdf5-c48114dd88b3 |
| Associated GPIs | 79750010002021 |
| GCN Sequence Number | 059910 |
| GCN Sequence Number Description | 0.9 % sodium chloride PGGYBK PRT INTRAVEN |
| HIC3 | C1B |
| HIC3 Description | SODIUM/SALINE PREPARATIONS |
| GCN | 25839 |
| 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 | Hospira, 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 | NDA019465 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 00409-7101-67 (00409710167)
| NDC Package Code | 0409-7101-67 |
|---|---|
| Billing NDC | 00409710167 |
| Package | 10 POUCH in 1 CASE (0409-7101-67) / 5 BAG in 1 POUCH / 100 mL in 1 BAG (0409-7101-69) |
| Marketing Start Date | 2005-08-24 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |