NDC 50090-4285

Potassium Chloride

Potassium Chloride

Potassium Chloride is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Potassium Chloride.

Product ID50090-4285_0064b5ba-f772-4ecd-bb85-ee43786d7e7e
NDC50090-4285
Product TypeHuman Prescription Drug
Proprietary NamePotassium Chloride
Generic NamePotassium Chloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2017-06-01
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA018279
Labeler NameA-S Medication Solutions
Substance NamePOTASSIUM CHLORIDE
Active Ingredient Strength750 mg/1
Pharm ClassesPotassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 50090-4285-0

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4285-0)
Marketing Start Date2019-04-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-4285-2 [50090428502]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA authorized generic
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-30

NDC 50090-4285-3 [50090428503]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA authorized generic
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-30

NDC 50090-4285-0 [50090428500]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA authorized generic
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-30

NDC 50090-4285-1 [50090428501]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA authorized generic
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-30

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM CHLORIDE750 mg/1

OpenFDA Data

SPL SET ID:238ca94a-d9f0-4747-801d-3af879cf570f
Manufacturer
UNII

Pharmacological Class

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

NDC Crossover Matching brand name "Potassium Chloride" or generic name "Potassium Chloride"

NDCBrand NameGeneric Name
0121-0841Potassium ChloridePOTASSIUM CHLORIDE
0121-1680Potassium ChloridePOTASSIUM CHLORIDE
0121-2520Potassium ChloridePOTASSIUM CHLORIDE
68001-235Potassium ChloridePotassium Chloride
68001-259Potassium ChloridePotassium Chloride
68001-303Potassium ChloridePotassium Chloride
68001-367potassium chloridepotassium chloride
0409-7074Potassium ChloridePotassium Chloride
0409-6651POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
0409-7075Potassium ChloridePotassium Chloride
0409-6653POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
0409-6635POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
0409-7077Potassium ChloridePotassium Chloride
0409-7076Potassium ChloridePotassium Chloride
68071-1933Potassium ChloridePotassium Chloride
68071-3153Potassium ChloridePotassium Chloride
68071-3274Potassium ChloridePotassium Chloride
68071-4078Potassium ChloridePotassium Chloride
68071-4296Potassium ChloridePotassium Chloride
68071-4708Potassium ChloridePotassium Chloride
68071-4716potassium chloridepotassium chloride
68084-419potassium chloridepotassium chloride
68084-524Potassium ChloridePotassium Chloride
68084-632Potassium ChloridePotassium Chloride
68084-360Potassium ChloridePotassium Chloride
68151-0609Potassium ChloridePotassium Chloride
68180-799Potassium ChloridePotassium Chloride
68180-798Potassium ChloridePotassium Chloride
68382-701POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
68382-398Potassium ChloridePotassium Chloride
68382-702POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
68382-320Potassium ChloridePotassium Chloride
68382-600Potassium ChloridePotassium Chloride
68382-776Potassium ChloridePotassium Chloride
68462-357Potassium ChloridePotassium Chloride
68462-472potassium chloridepotassium chloride
68462-471potassium chloridepotassium chloride
68788-6771Potassium ChloridePotassium Chloride
68788-6772Potassium ChloridePotassium Chloride
69238-1458Potassium ChloridePotassium Chloride
69238-1459Potassium ChloridePotassium Chloride
0574-0181Potassium ChloridePotassium Chloride
0574-0180Potassium ChloridePotassium Chloride
70436-001Potassium ChloridePotassium Chloride
70518-0057Potassium ChloridePotassium Chloride
70518-0152Potassium ChloridePotassium Chloride
70518-0348Potassium ChloridePotassium Chloride
70436-002Potassium ChloridePotassium Chloride
70518-1068Potassium ChloridePotassium Chloride
70518-1203Potassium ChloridePotassium Chloride

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.