Lithium 8 meq/5mL
Lithium · SOLUTION · PAI Holdings, LLC dba PAI Pharma
Lithium is a solution containing lithium at 8 meq/5mL, taken oral. Manufactured by PAI Holdings, LLC dba PAI Pharma.
Key Facts
- Brand Name
- Lithium
- Generic Name
- Lithium
- NDC Code (Product)
0121-4027- Manufacturer
- PAI Holdings, LLC dba PAI Pharma
- Strength
- 8 meq/5mL
- Dosage Form
- SOLUTION
- Route
- ORAL
- Marketing Status
- Application #
- ANDA070755
- Marketing Start
- 04/14/2026
Recall History
Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
CARDINAL HEALTHCARE
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Tri-Coast Pharmacy
Lack of Assurance of Sterility
Aidapak Services, LLC
Labeling: Label Mixup: LITHIUM CARBONATE ER, Tablet, 450 mg may be potentially mislabled as one of the following drugs: HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, NDC 00574025001, Pedigree: AD21790_19, EXP: 5/1/2014; LACTOBACILLUS ACIDOPHILUS, Capsule, 500 MILLION CFU, NDC 43292050022, Pedigree: AD46257_28, EXP: 5/15/2014; HYDROCORTISONE, Tablet, 5 mg, NDC 00603389919, Pedigree: W002729, EXP: 6
Franck's Lab Inc., d.b.a. Franck's Compounding Lab
Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012. FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.
Aidapak Services, LLC
Labeling: Label Mixup: LITHIUM CARBONATE ER, Tablet, 225 mg (1/2 of 450 mg) may be potentially mislabled as one of the following drugs: CYCLOBENZAPRINE HCL, Tablet, 5 mg, NDC 00591325601, Pedigree: AD73525_7, EXP: 5/30/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: AD21846_11, EXP: 5/1/2014.
Aidapak Services, LLC
Labeling: Label Mixup: LITHIUM CARBONATE ER, Tablet, 300 mg may be potentially mislabled as the following drug: VITAMIN B COMPLEX PROLONGED RELEASE, Tablet, 50 mg, NDC 40985022251, Pedigree: AD39588_10, EXP: 5/13/2014.
Side Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is Lithium used for?
Lithium contains Lithium. It is a solution taken oral. Consult your doctor for specific uses.
Is Lithium a controlled substance?
Lithium is not classified as a controlled substance by the DEA.
What is the generic name for Lithium?
The generic name for Lithium is Lithium. There are 12 other brand versions of Lithium.
What is the NDC code for Lithium 8 meq/5mL?
The NDC (National Drug Code) for Lithium 8 meq/5mL is 0121-4027, listed by PAI Holdings, LLC dba PAI Pharma.
Other Lithium Brands
See all →- Lithium Carbonate600 mg/172789-172
- Lithium Carbonicum500 [hp_C]/137662-0940
- Lithium Carbonicum1 [hp_M]/137662-0941
- Lithium Bromatum6 [hp_C]/137662-1061
- Lithium Bromatum30 [hp_C]/137662-1063
- Lithium Bromatum500 [hp_C]/137662-1066
- Lithium Muriaticum12 [hp_C]/137662-1514
- Lithium Oxydatum100 [hp_C]/137662-2680
- Lithium Phosphoricum1 [hp_M]/137662-2691
- Lithium Phosphoricum500 [hp_C]/137662-2795
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)