NDC 0074-3058

K-Tab

Potassium Chloride

K-Tab is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is Potassium Chloride.

• Product ID: 0074-3058_269b29d0-1d90-1622-ef7d-d54f7bd47409
• NDC: 0074-3058
• Product Type: Human Prescription Drug
• Proprietary Name: K-Tab
• Generic Name: Potassium Chloride
• Dosage Form: Tablet, Film Coated, Extended Release
• Route of Administration: ORAL
• Marketing Start Date: 1980-06-09
• Marketing Category: NDA / NDA
• Application Number: NDA018279
• Labeler Name: AbbVie Inc.
• 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 0074-3058-41

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-3058-41)

• Marketing Start Date: 1980-06-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0074-3058-30 [00074305830]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA018279
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-09-30
• Marketing End Date: 2017-07-10

NDC 0074-3058-41 [00074305841]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA018279
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1980-06-09

NDC 0074-3058-90 [00074305890]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA018279
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-09-30
• Marketing End Date: 2017-07-10

NDC 0074-3058-46 [00074305846]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA018279
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1980-06-09

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM CHLORIDE	600 mg/1

OpenFDA Data

• SPL SET ID: 6594df99-d8ce-49b9-3fbe-9ec7cdc9199b
• Manufacturer:
  • AbbVie Inc.
• UNII:
  • 660YQ98I10
• RxNorm Concept Unique ID - RxCUI:
  • 312529
  • 1541594
  • 628953
  • 198116
  • 670031
  • 1483340
• UPC Code:
  • 0300743023138
  • 0300743278132
  • 0300743058413
  • 0300747804191

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 "K-Tab" or generic name "Potassium Chloride"

NDC	Brand Name	Generic Name
0074-3023	K-Tab	Potassium Chloride
0074-3058	K-Tab	Potassium Chloride
0074-3278	K-Tab	Potassium Chloride
0074-7804	K-Tab	Potassium Chloride
70518-0220	K-Tab	K-Tab
43353-790	K-Tab	K-Tab
53808-0277	K-TAB	K-TAB
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