NDC 0245-5315

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 Upsher-smith Laboratories, Llc. The primary component is Potassium Chloride.

• Product ID: 0245-5315_0907ea1c-82f3-4ba8-9d1b-3f4fa104d7a2
• NDC: 0245-5315
• 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: Upsher-Smith Laboratories, 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: 2021-12-31

Packaging

NDC 0245-5315-01

100 BLISTER PACK in 1 BLISTER PACK (0245-5315-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0245-5315-89)

• Marketing Start Date: 2019-06-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0245-5315-89 [00245531589]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1986-04-17

NDC 0245-5315-11 [00245531511]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-06-21

NDC 0245-5315-01 [00245531501]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-06-21

NDC 0245-5315-15 [00245531515]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA019123
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-06-21

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM CHLORIDE	600 mg/1

OpenFDA Data

• SPL SET ID: 1ff53330-065c-4213-9c0c-ac498621d09d
• Manufacturer:
  • Upsher-Smith Laboratories, LLC
• UNII:
  • 660YQ98I10
• UPC Code:
  • 0302455316119
  • 0302455315112

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