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Sodium Chloride 0.9% ADD-Vantage Diluent Bags
Manufacturer:
PFIZER INC.
Regulated product
Non-Returnable Product
Manufacturer:
PFIZER INC.
Product description:
Always follow your local protocols regarding product use.
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Preservative-Free
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Latex Free
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Product # | 0409-7101-66 | 0409-7101-67 | 00409-7101-02 |
Strength | 0.9% | 0.9% | |
Color | Colorless | Colorless | |
Application Type | Human Prescription Drug | Human Prescription Drug | |
Purpose | Replacement Preparation | Replacement Preparation | |
Route of Administration | Intravenous | Intravenous | |
Preservative-Free | Yes | Yes | |
Concentration | 0.9% | ||
pH Range | 5.6 (4.5 to 7.0) | 5.6 (4.5 to 7.0) | |
User Type | Indicated For Parenteral Replenishment of Fluid and Sodium Chloride as Required by the Clinical Condition of the Patient | Indicated For Parenteral Replenishment of Fluid and Sodium Chloride as Required by the Clinical Condition of the Patient | |
Life Stage | 100mL | 250mL | |
NDC | 0409-7101-67 | 00409-7101-02 | |
Grade | Usp | Usp | Usp |
Sterile | Sterile | Sterile | |
Container Type | ADD-vantage Flexible Container | ||
Formulation | Liquid/Injection Solution | Liquid/Injection Solution | |
Storage Requirements | 20 to 25°C, USP Controlled Room Temperature, Protect From Freezing | 20 to 25°C, USP Controlled Room Temperature, Protect From Freezing | |
Uses | This Parenteral Preparation is Indicated Only for Diluting or Dissolving Drugs for Intravenous, Intramuscular or Subcutaneous Injection, According to Instructions of the Manufacturer of the Drug to be Administered, as Diluent | This Parenteral Preparation is Indicated Only for Diluting or Dissolving Drugs for Intravenous, Intramuscular or Subcutaneous Injection, According to Instructions of the Manufacturer of the Drug to be Administered, as Diluent | |
Latex Free | Yes | ||
Brand | ADD-Vantage | ||
Active Ingredient | Sodium, Chloride | Sodium, Chloride |