NDC 44523-410 – Potassium Citrate

Potassium Citrate 10 meq/1 · Tablet · Oral

Human Prescription Drug

Product NDC44523-410

Product details

Brand name
Potassium Citrate
Generic name
Potassium citrate
Labeler
Biocomp Pharma, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA019071
Marketed since
December 3, 2024
Listing expires
December 31, 2026
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent

Active ingredients

Uses, dosage, side effects and warnings for Potassium Citrate →

Package NDC codes (1)

Package NDCDescriptionSince
44523-410-01100 TABLET in 1 BOTTLE (44523-410-01)Dec 3, 2024

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