Potassium Chloride

Product NDC
71610-977
11-digit product format
716100977
Labeler code
71610
Product ID
71610-977_471f3a17-baa9-cc35-e063-6294a90aed96
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA218979
Marketing category
ANDA
Marketing start
2025-08-08
Substance
POTASSIUM CHLORIDE
Active strength
750 mg/1
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
660YQ98I10POTASSIUM CHLORIDE7447-40-7POTASSIUM CHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71610-977-307161009773030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-30) 2025-12-29NoNoHistorical
71610-977-537161009775360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-53) 2025-12-29NoNoHistorical
71610-977-607161009776090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-60) 2025-12-29NoNoHistorical
71610-977-7071610097770120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-70) 2025-12-29NoNoHistorical
71610-977-7371610097773135 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-73) 2025-12-29NoNoHistorical
71610-977-8071610097780180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-80) 2025-12-29NoNoHistorical
71610-977-8571610097785200 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-85) 2025-12-29NoNoHistorical
71610-977-9271610097792270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-92) 2025-12-29NoNoHistorical
71610-977-9471610097794360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-977-94) 2025-12-29NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Potassium ChlorideAphena Pharma Solutions - Tennessee, LLC2025-12-29HUMAN PRESCRIPTION DRUG LABEL1