NDC 0245-5317

KLOR-CON M

Potassium Chloride

KLOR-CON M is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Upsher-smith Laboratories, Llc. The primary component is Potassium Chloride.

Product ID0245-5317_880b7537-b866-4d8b-8f13-465d8d3a23e4
NDC0245-5317
Product TypeHuman Prescription Drug
Proprietary NameKLOR-CON M
Generic NamePotassium Chloride
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2011-01-18
Marketing CategoryANDA / ANDA
Application NumberANDA074726
Labeler NameUpsher-Smith Laboratories, LLC
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 0245-5317-01

100 BLISTER PACK in 1 CARTON (0245-5317-01) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0245-5317-89)
Marketing Start Date2019-06-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0245-5317-90 [00245531790]

KLOR-CON M TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074726
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-21

NDC 0245-5317-01 [00245531701]

KLOR-CON M TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074726
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-21

NDC 0245-5317-10 [00245531710]

KLOR-CON M TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074726
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-21

NDC 0245-5317-89 [00245531789]

KLOR-CON M TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074726
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-01-18

NDC 0245-5317-11 [00245531711]

KLOR-CON M TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074726
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-21

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM CHLORIDE750 mg/1

OpenFDA Data

SPL SET ID:b89910f6-4ff5-4a62-8269-696f7c10e4f6
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]

NDC Crossover Matching brand name "KLOR-CON M" or generic name "Potassium Chloride"

NDCBrand NameGeneric Name
70518-1899KLOR-CON MKLOR-CON M
0615-7862KLOR-CON MKLOR-CON M
0615-7861KLOR-CON MKLOR-CON M
43353-797Klor-Con MKlor-Con M
43353-988KLOR-CON MKLOR-CON M
43353-990KLOR-CON MKLOR-CON M
0245-0058Klor-Con MKlor-Con M
0245-0057Klor-Con MKlor-Con M
0245-0150Klor-Con MKlor-Con M
55154-0926KLOR-CON MKLOR-CON M
55154-0928KLOR-CON MKLOR-CON M
55289-444Klor-Con MKlor-Con M
63629-6534KLOR-CON MKLOR-CON M
66758-180KLOR-CON MKLOR-CON M
66758-190KLOR-CON MKLOR-CON M
66758-170KLOR-CON MKLOR-CON M
67544-349Klor-Con MKlor-Con M
0245-5318KLOR-CON MKLOR-CON M
0245-5317KLOR-CON MKLOR-CON M
0245-5319KLOR-CON MKLOR-CON M
70518-2558KLOR-CON MKLOR-CON M
0074-3023K-TabPotassium Chloride
0074-3058K-TabPotassium Chloride
0074-3278K-TabPotassium Chloride
0074-7804K-TabPotassium Chloride
0220-2891Kali muriaticumPOTASSIUM CHLORIDE
0220-2951Kali muriaticumPOTASSIUM CHLORIDE
0220-2952Kali muriaticumPOTASSIUM CHLORIDE
0220-2953Kali muriaticumPOTASSIUM CHLORIDE
0220-2954Kali muriaticumPOTASSIUM CHLORIDE
0220-2955Kali muriaticumPOTASSIUM CHLORIDE
0220-2956Kali muriaticumPOTASSIUM CHLORIDE
0220-2957Kali muriaticumPOTASSIUM CHLORIDE
0121-0841Potassium ChloridePOTASSIUM CHLORIDE
0121-1680Potassium ChloridePOTASSIUM CHLORIDE
0121-2520Potassium ChloridePOTASSIUM CHLORIDE

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