NDC 67544-154

Klor-Con

Potassium Chloride

Klor-Con is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Aphena Pharma Solutions - Tennessee, Llc. The primary component is Potassium Chloride.

• Product ID: 67544-154_c3fb8c8c-fa8d-4890-a843-1999add4d22b
• NDC: 67544-154
• Product Type: Human Prescription Drug
• Proprietary Name: Klor-Con
• Generic Name: Potassium Chloride
• Dosage Form: Tablet, Film Coated, Extended Release
• Route of Administration: ORAL
• Marketing Start Date: 1986-04-17
• Marketing Category: NDA / NDA
• Application Number: NDA019123
• Labeler Name: Aphena Pharma Solutions - Tennessee, LLC
• Substance Name: POTASSIUM CHLORIDE
• Active Ingredient Strength: 600 mg/1
• Pharm Classes: 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 Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 67544-154-80

180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (67544-154-80)

• Marketing Start Date: 1986-04-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 67544-154-60 [67544015460]

Klor-Con TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-07-23
• Marketing End Date: 2019-04-18

NDC 67544-154-53 [67544015453]

Klor-Con TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-08-24
• Marketing End Date: 2019-04-18

NDC 67544-154-94 [67544015494]

Klor-Con TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-06-05
• Marketing End Date: 2019-04-18

NDC 67544-154-80 [67544015480]

Klor-Con TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-07-04
• Marketing End Date: 2019-04-18

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM CHLORIDE	600 mg/1

OpenFDA Data

• SPL SET ID: fde63a82-6a2a-478d-b3d9-41b8f147e0dd
• Manufacturer:
  • Aphena Pharma Solutions - Tennessee, LLC
• UNII:
  • 660YQ98I10
• RxNorm Concept Unique ID - RxCUI:
  • 832718
  • 628958
  • 312529
  • 628953

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" or generic name "Potassium Chloride"

NDC	Brand Name	Generic Name
0440-8110	Klor-Con	Klor-Con
0615-8045	KLOR-CON	KLOR-CON
43353-064	KLOR-CON	KLOR-CON
0245-0041	Klor-Con	Klor-Con
0245-0040	Klor-Con	Klor-Con
0245-0360	KLOR-CON	KLOR-CON
55154-0927	KLOR-CON	KLOR-CON
55289-697	Klor-Con	Klor-Con
65084-464	KLOR-CON	KLOR-CON
65084-465	KLOR-CON	KLOR-CON
66758-160	KLOR-CON	KLOR-CON
66758-110	KLOR-CON	KLOR-CON
67544-237	Klor-Con	Klor-Con
67544-154	Klor-Con	Klor-Con
0245-5315	KLOR-CON	KLOR-CON
0245-5316	KLOR-CON	KLOR-CON
0074-3023	K-Tab	Potassium Chloride
0074-3058	K-Tab	Potassium Chloride
0074-3278	K-Tab	Potassium Chloride
0074-7804	K-Tab	Potassium Chloride
0220-2891	Kali muriaticum	POTASSIUM CHLORIDE
0220-2951	Kali muriaticum	POTASSIUM CHLORIDE
0220-2952	Kali muriaticum	POTASSIUM CHLORIDE
0220-2953	Kali muriaticum	POTASSIUM CHLORIDE
0220-2954	Kali muriaticum	POTASSIUM CHLORIDE
0220-2955	Kali muriaticum	POTASSIUM CHLORIDE
0220-2956	Kali muriaticum	POTASSIUM CHLORIDE
0220-2957	Kali muriaticum	POTASSIUM CHLORIDE
0121-0841	Potassium Chloride	POTASSIUM CHLORIDE
0121-1680	Potassium Chloride	POTASSIUM CHLORIDE
0121-2520	Potassium Chloride	POTASSIUM CHLORIDE