6505-01-373-2802

Description: Dantrolene Sodium For Injection

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MILSPEC: Drugs And Biologicals

 Export Restrictions

Any part(s) quoted or sold by MilSpec.parts and re-sold (to a third party) CANNOT be sold to a USA embargoed country, company, entity, or person(s). Depending on the ECCN, these commodities may require export license or exception. Diversion contrary to U.S. law is prohibited. Unless otherwise noted, this sale, order or quote may include Munitions List Items (MLI) or Commerce Controlled List Items (CCLI). MLI/CCLI property is controlled by the US Government and in many cases cannot be transferred (exported, sold or given) to a foreign country, a non-US Citizen/National or a non- Permanent US Resident without a valid State/Commerce Department export authorization. It is the responsibility of (the Purchaser) to determine what the applicable requirements may be, to obtain all necessary authorizations, licenses or approvals and are subject to both review and acceptance by MilSpec.parts. The use, disposition, export and re-export of the property covered or included in this sale, order or quote is subject to the provisions of law referenced in End-Use Certificate DLA form 1822, DEC 2001, including, but not limited to, the Arms Export Control Act (22 USC 2751 et seq.); Export Administration Act of 1979 (50 USC App. 2401 et seq.) as contained under Executive Order 12924; International Traffic in Arms Regulations (22 CFR 120 et seq.); Export Administration Regulations (15 CFR 730 et seq.); Foreign Assets Control Regulations (31 CFR 500 et seq.) and the Espionage Act (18 USC 793 et seq.)

6505-01-373-2802 Properties

  • NSN:
    6505-01-373-2802
  • Description:
    Dantrolene Sodium For Injection
  • Shelf Life:
    > 60 mo.
  • DEMIL:
    NO
  • UOM:
    PG
  • Physical Form:
    Powder
  • Active Medicament Medicinal Strength:
    20.000 milligrams dantrolene sodium active ingredient
  • Primary Container Type:
    Vial
  • Primary Container Content Quantity:
    20 milligrams active ingredient
  • Total Primary Container Quantity:
    6
  • Administration:
    Intravenous
  • Special Features:
    Contains 3000 mg mannito and sufficient sodium hydroxide to yield a ph of approx. 9.5; for reconstitution water for injection without bacteriostatic agent; for treatment of malignant hyperthermia
Manufacturers and Part Numbers
Part Number
Brand
NDC00149-0734-02
Procter & Gamble Pharmaceuticals
73402
Procter & Gamble Pharmaceuticals
Major Organizational Entities (MOE)
Entity
MOE Code
MOE Rule
PICA
DSOR
User:
VETERANS ADMINISTRATION Veterans Administration
MOE_CD:
VA
MOE_RL:
V542
PICA:
54
DSOR:
Part Identification
INC
FIIG
Concept No.
App. Key
Cond. Code
Status
INC:
37569
FIIG:
A34300
Concept No.:
App. Key:
A
Cond. Code:
1
Status:
A
Material and Special Handling
Hazardous material, precious metals, criticality, enviroment, and electrostatic discharge indicators
HMIC
PMIC
ESD/EMI
ENAC
MMAC
CRITL
HMIC:
P
PMIC:
A
ESD:
ESD:
MMAC:
---
CRITL:
X
Hazmat (HMIC): P
Indicates there is no information in the hmirs. The nsn is in a fsc in table ii of fed std 313 and a msds may be required by the user. The requirement for a msds is dependent on a hazard determination of the supplier or the intended end use of item.
Precious Metals (PMIC): A
Item does not contain precious metal.
Criticality (CRITL): X
The item does not have a nuclear hardened feature or any other critical feature such as tolerance, fit restriction or application.
Packaging and Dimensions
Package Size
Package Weight
Part Weight
Part Dimensions (approx.)
Pack Size:
--
Pack Weight:
--
Item Weight:
--
Item Dim:
--
Container
OPI
SPI No.
SPI Rev.
Container:
OPI:
SPI No.:
SPI Rev.:
SPC Mkg.
LVL A
LVL B
LVL C
SPC Mkg.:
LVL A:
LVL B:
LVL C:
CUSH
MOP
CATEG.
PRESS MAT
CUSH:
MOP:
CATEG.:
PRESS MAT:
WRAP MAT
ICQ
THK
TOS
UCL
WRAP MAT:
ICQ:
THK:
TOS:
UCL:
Packaging Code Definitions
LVL A Code (LVL_A):
LVL B Code (LVL_B):
Procedure Indicator Code (OPI):
Special Markings Code (SPC MKG):
Method of Preservation (MOP):
Cushion Material (CUSH):
Preservation Material (PRESS MAT):