United States · FDA National Drug Code directory
Lithium
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
- 71656-072_3ccc30e9-1f5d-5715-e063-6394a90a6bc1
- Product NDC
- 71656-072
- Form
- SOLUTION
- Composition / generic term
- Lithium
- Labeler
- Saptalis Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240328
- Source listing expiry
- 20261231
Source-listed ingredients
- LITHIUM CITRATE — 8 meq/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (71656-072-16) · 71656-072-16
- 5 TRAY in 1 CASE (71656-072-50) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (71656-072-05) · 71656-072-50
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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