Pill Identifier Lithium Carbonate - NDC 68462-223
Lithium Carbonate
Product Code 68462-223
Lithium Carbonate by Glenmark Pharmaceuticals Inc., Usa is a pink rou tablet film coated extended release about 10 mm in size, imprinted with 223;plain. The product is a human prescription drug with active ingredient(s) lithium carbonate.
Lithium Carbonate
Active Ingredient(s): Lithium Carbonate
Inactive Ingredient(s):
- SODIUM CHLORIDE
- POVIDONE K30
- SORBITOL
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- CALCIUM STEARATE
- SODIUM LAURYL SULFATE
- HYPROMELLOSE 2910 (15000 MPA.S)
- TITANIUM DIOXIDE
- POLYETHYLENE GLYCOL 400
- FERRIC OXIDE RED

Image of Lithium Carbonate tablet, film coated, extended release by Glenmark Pharmaceuticals Inc., Usa
Glenmark Pharmaceuticals Inc., Usa
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Pink (C48328)
Product Packages
NDC Package Code | Package Description |
---|---|
68462-223-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
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Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.