NDC 0338-0049

Sodium Chloride

Sodium Chloride

Sodium Chloride is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Sodium Chloride.

Product ID0338-0049_12f9ba39-2971-4f47-b9d1-073847c04353
NDC0338-0049
Product TypeHuman Prescription Drug
Proprietary NameSodium Chloride
Generic NameSodium Chloride
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date1970-12-09
Marketing CategoryNDA / NDA
Application NumberNDA016677
Labeler NameBaxter Healthcare Corporation
Substance NameSODIUM CHLORIDE
Active Ingredient Strength9 g/1000mL
Pharm ClassesOsmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0338-0049-01

150 mL in 1 BAG (0338-0049-01)
Marketing Start Date1970-12-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0338-0049-11 [00338004911]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-04 [00338004904]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-31 [00338004931]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-10 [00338004910]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-38 [00338004938]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-01 [00338004901]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-03 [00338004903]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-18 [00338004918]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-41 [00338004941]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-48 [00338004948]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

NDC 0338-0049-02 [00338004902]

Sodium Chloride INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA016677
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1970-12-09

Drug Details

Active Ingredients

IngredientStrength
SODIUM CHLORIDE9 g/1000mL

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 "Sodium Chloride" or generic name "Sodium Chloride"

NDCBrand NameGeneric Name
0019-1188SODIUM CHLORIDEsodium chloride
0264-1800Sodium ChlorideSodium Chloride
0264-2201Sodium ChlorideSodium Chloride
0264-5802Sodium ChlorideSODIUM CHLORIDE
0264-5804Sodium ChlorideSODIUM CHLORIDE
0264-7800Sodium ChlorideSodium Chloride
0264-7802Sodium ChlorideSODIUM CHLORIDE
0264-7805Sodium ChlorideSodium Chloride
0264-7806Sodium ChlorideSodium Chloride
0264-9375Sodium ChlorideSodium Chloride
0264-9999Sodium ChlorideSodium Chloride
0338-0043Sodium ChlorideSodium Chloride
0409-4888Sodium ChlorideSodium Chloride
0409-6138Sodium ChlorideSodium Chloride
0409-6660Sodium ChlorideSodium Chloride
0409-7101Sodium ChlorideSodium Chloride
0409-7138Sodium ChlorideSodium Chloride
0409-7132Sodium ChlorideSodium Chloride
0409-7972Sodium ChlorideSodium Chloride
0409-7983Sodium ChlorideSodium Chloride
0409-7984Sodium ChlorideSodium Chloride
0409-7730Sodium ChlorideSodium Chloride
0409-7985Sodium ChlorideSodium Chloride
0487-9301Sodium ChlorideSodium Chloride
0517-2810Sodium ChlorideSodium Chloride
70518-1425Sodium ChlorideSodium Chloride
76297-001Sodium ChlorideSodium Chloride
0641-1512Sodium ChlorideSodium Chloride
0641-0497Sodium ChlorideSodium Chloride
0641-6144Sodium ChlorideSodium Chloride
0990-7984Sodium ChlorideSodium Chloride
11822-5458Sodium ChlorideSodium Chloride
17238-625Sodium ChlorideSodium Chloride
17271-701Sodium chlorideSodium chloride
17478-622Sodium ChlorideSodium Chloride
17478-623Sodium ChlorideSodium Chloride
46163-300Sodium ChlorideSodium Chloride
49230-300Sodium ChlorideSodium Chloride
50090-2488Sodium ChlorideSodium Chloride
51662-1342SODIUM CHLORIDESODIUM CHLORIDE
51662-1258SODIUM CHLORIDESODIUM CHLORIDE
51662-1318SODIUM CHLORIDESODIUM CHLORIDE
52584-025Sodium ChlorideSodium Chloride
52584-888Sodium ChlorideSodium Chloride
55154-6979Sodium ChlorideSodium Chloride
55154-0126Sodium ChlorideSodium Chloride
0220-0432Aqua marinaSODIUM CHLORIDE
0220-3582Natrum muriaticumSODIUM CHLORIDE
0220-3583Natrum muriaticumSODIUM CHLORIDE
0220-3586Natrum muriaticumSODIUM CHLORIDE
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.