NDC 49281-912

Diluent

Sodium Chloride

Diluent is a Subcutaneous Injection in the Vaccine category. It is labeled and distributed by Sanofi Pasteur Inc.. The primary component is Sodium Chloride.

Product ID49281-912_23bda4a7-a1c1-4390-8da8-df0de0698a53
NDC49281-912
Product TypeVaccine
Proprietary NameDiluent
Generic NameSodium Chloride
Dosage FormInjection
Route of AdministrationSUBCUTANEOUS
Marketing Start Date1953-05-22
Marketing CategoryBLA / BLA
Application NumberBLA103915
Labeler NameSanofi Pasteur Inc.
Substance NameSODIUM CHLORIDE
Active Ingredient Strength5 mg/.5mL
Pharm ClassesOsmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49281-912-05

5 VIAL, SINGLE-DOSE in 1 PACKAGE (49281-912-05) > .6 mL in 1 VIAL, SINGLE-DOSE (49281-912-59)
Marketing Start Date1953-05-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49281-912-69 [49281091269]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22

NDC 49281-912-03 [49281091203]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22
Marketing End Date2016-06-12

NDC 49281-912-01 [49281091201]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22
Marketing End Date2016-06-12

NDC 49281-912-10 [49281091210]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22

NDC 49281-912-05 [49281091205]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22

NDC 49281-912-58 [49281091258]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22
Marketing End Date2016-06-12

NDC 49281-912-68 [49281091268]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22
Marketing End Date2016-06-12

NDC 49281-912-59 [49281091259]

Diluent INJECTION
Marketing CategoryBLA
Application NumberBLA103915
Product TypeVACCINE
Marketing Start Date1953-05-22

Drug Details

Active Ingredients

IngredientStrength
SODIUM CHLORIDE4.5 mg/.5mL

Pharmacological Class

  • Osmotic Laxative [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Osmotic Activity [MoA]

NDC Crossover Matching brand name "Diluent" or generic name "Sodium Chloride"

NDCBrand NameGeneric Name
0173-0518Diluentwater
0173-0857Diluentwater
0781-6021DILUENTDILUENT
49281-912DiluentDiluent
0220-0432Aqua marinaSODIUM CHLORIDE
0220-3582Natrum muriaticumSODIUM CHLORIDE
0220-3583Natrum muriaticumSODIUM CHLORIDE
0220-3586Natrum muriaticumSODIUM CHLORIDE
0220-3587Natrum muriaticumSODIUM CHLORIDE
0220-3590Natrum muriaticumSODIUM CHLORIDE
0220-3593Natrum muriaticumSODIUM CHLORIDE
0220-3595Natrum muriaticumSODIUM CHLORIDE
0220-3596Natrum muriaticumSODIUM CHLORIDE
0220-3597Natrum muriaticumSODIUM CHLORIDE
0220-3598Natrum muriaticumSODIUM CHLORIDE
0220-3599Natrum muriaticumSODIUM CHLORIDE
0220-3600Natrum muriaticumSODIUM CHLORIDE
0220-3601Natrum muriaticumSODIUM CHLORIDE
0019-1188SODIUM CHLORIDEsodium chloride
0264-1800Sodium ChlorideSodium Chloride
0264-2201Sodium ChlorideSodium Chloride
0264-5802Sodium ChlorideSODIUM CHLORIDE
0264-5804Sodium ChlorideSODIUM CHLORIDE
0264-7800Sodium ChlorideSodium Chloride
0002-0800Sterile Diluentdiluent

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