United States · FDA National Drug Code directory
Quinidine Gluconate
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
- 53489-141_47cec250-341a-4694-a232-93106833a75e
- Product NDC
- 53489-141
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Quinidine Gluconate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19870210
- Source listing expiry
- 20261231
Source-listed ingredients
- QUINIDINE GLUCONATE — 324 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-01) · 53489-141-01
- 250 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-03) · 53489-141-03
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-05) · 53489-141-05
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-06) · 53489-141-06
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-07) · 53489-141-07
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-10) · 53489-141-10
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-141-90) · 53489-141-90
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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