NDC 71656-072 – Lithium

Lithium Citrate 8 meq/5mL · Solution · Oral

Human Prescription Drug

Product NDC71656-072

Product details

Brand name
Lithium
Generic name
Lithium
Labeler
Saptalis Pharmaceuticals, LLC
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA217183
Marketed since
March 28, 2024
Listing expires
December 31, 2026
Pharmacologic class
Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Lithium →

Package NDC codes (2)

Package NDCDescriptionSince
71656-072-16473 mL in 1 BOTTLE (71656-072-16)Apr 5, 2024
71656-072-505 TRAY in 1 CASE (71656-072-50) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (71656-072-05)Mar 28, 2024

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