United States · FDA National Drug Code directory

Potassium Citrate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 68084-850_213c9f49-5d37-f84f-e063-6394a90aa698
Product NDC: 68084-850
Form: TABLET, EXTENDED RELEASE
Composition / generic term: Potassium Citrate
Labeler: American Health Packaging
Marketing category: ANDA
Marketing start / end (source format): 20141112
Source listing expiry: 20261231

Source-listed ingredients

POTASSIUM CITRATE — 10 meq/1

These values do not establish equivalence or a dose recommendation.

Packages

20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-850-32) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-850-33) · 68084-850-32

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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